NP-MRD: Showing NP-Card for 4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde (NP0289601)

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Record Information

Version

2.0

Created at

2022-09-09 19:52:22 UTC

Updated at

2022-09-09 19:52:22 UTC

NP-MRD ID

NP0289601

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde

Description

4-Hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0³,⁷]Trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde belongs to the class of organic compounds known as benzophenones. These are organic compounds containing a ketone attached to two phenyl groups. Based on a literature review very few articles have been published on 4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0³,⁷]Trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092221522D          

 30 33  0  0  0  0            999 V2000
    6.2102   -3.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -2.6021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -1.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246   -0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.5396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8371    0.2900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    2.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -2.6021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 20 26  1  0  0  0  0
 26 27  1  0  0  0  0
 17 27  1  0  0  0  0
  8 28  2  0  0  0  0
  3 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
M  END

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
    5.1512    2.8591    1.2539 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3999    2.1937    0.2778 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7043    1.0039    0.5118 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7108    0.3908    1.7479 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9941   -0.7823    1.8823 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9796   -1.4199    3.1036 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3041   -1.3048    0.8081 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2940   -0.6914   -0.4369 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6252   -1.2234   -1.6076 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3769   -1.3724   -2.6281 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2330   -1.5603   -1.6299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2444   -2.2629   -2.7378 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6564   -2.6116   -3.7153 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5826   -2.5573   -2.7739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4394   -2.1788   -1.7584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8945   -2.5018   -1.8001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9560   -1.4832   -0.6669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6012   -1.1724   -0.6080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2126   -0.4755    0.5118 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0084    0.4591    1.1792 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5202    0.5622    2.6242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7872    1.7108    0.5923 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7543    1.8817   -0.3629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0058    1.3760    0.3206 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5328    2.4093    1.2762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4707    0.1967    1.1053 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8530   -1.0739    0.4213 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0158    0.4831   -0.5602 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0314    1.1625   -1.8640 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9458    0.8277   -2.6518 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9076    3.5437    0.8119 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4385    3.4246    1.9041 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7183    2.1707    1.9226 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2756    0.8658    2.5332 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4751   -1.0550    3.8981 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7634   -2.2328    0.9450 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4045   -3.1167   -4.5470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9882   -3.0931   -3.6022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0771   -3.0928   -2.7205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1892   -3.1599   -0.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5072   -1.5893   -1.8762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3989    0.3076    3.2788 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3089   -0.1348    2.8091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2295    1.5899    2.8946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5104    1.2615   -1.2545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8166    2.9644   -0.5958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7749    1.0508   -0.4122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7026    3.1332    1.4809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3600    3.0012    0.8464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8127    1.9274    2.2491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9046    0.2373    2.1193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0435   -1.8629    1.1756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8599   -0.8856   -0.0571 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3242    1.9001   -2.1562 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  1
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
  8 28  2  0
 28 29  1  0
 29 30  2  0
 28  3  1  0
 18 11  1  0
 26 20  1  0
 27 17  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
  6 35  1  0
  7 36  1  0
 13 37  1  0
 14 38  1  0
 16 39  1  0
 16 40  1  0
 16 41  1  0
 21 42  1  0
 21 43  1  0
 21 44  1  0
 23 45  1  0
 23 46  1  0
 24 47  1  6
 25 48  1  0
 25 49  1  0
 25 50  1  0
 26 51  1  1
 27 52  1  0
 27 53  1  0
 29 54  1  0
M  END


  Mrv1652309092221522D          

 30 33  0  0  0  0            999 V2000
    6.2102   -3.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -2.6021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -1.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246   -0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.5396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8371    0.2900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    2.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -2.6021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 20 26  1  0  0  0  0
 26 27  1  0  0  0  0
 17 27  1  0  0  0  0
  8 28  2  0  0  0  0
  3 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0289601

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(O)=CC(C(=O)C2=C(O)C=C(C)C3=C2OC2(C)OCC(C)C2C3)=C1C=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H24O7/c1-11-5-18(26)20(21(27)15-6-13(25)7-19(28-4)16(15)9-24)22-14(11)8-17-12(2)10-29-23(17,3)30-22/h5-7,9,12,17,25-26H,8,10H2,1-4H3

> <INCHI_KEY>
CCRDXZGFEZQDRL-UHFFFAOYSA-N

> <FORMULA>
C23H24O7

> <MOLECULAR_WEIGHT>
412.438

> <EXACT_MASS>
412.152203113

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
42.55293752410937

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0^{3,7}]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde

> <JCHEM_LOGP>
4.539533908333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.674009630278751

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.767115713795637

> <JCHEM_PKA_STRONGEST_BASIC>
-4.171439125159854

> <JCHEM_POLAR_SURFACE_AREA>
102.29

> <JCHEM_REFRACTIVITY>
111.12719999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0^{3,7}]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      11.592  -5.627   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      10.259  -4.857   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      10.259  -3.317   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.592  -2.547   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.592  -1.007   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      12.926  -0.237   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      10.259  -0.237   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.925  -1.007   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.591  -0.237   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.258  -1.007   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       7.591   1.303   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.925   2.073   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      10.259   1.303   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.925   3.613   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.591   4.383   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.591   5.923   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.924   1.303   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.429   0.541   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.126   1.597   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.126   4.089   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.650   5.553   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.925  -2.547   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.591  -3.317   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       7.591  -4.857   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   28                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   28                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   18                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   27                                                  
CONECT   18   17   11   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22   26                                             
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   20   27                                                  
CONECT   27   26   17                                                       
CONECT   28    8    3   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₄O₇

Average Mass

412.4380 Da

Monoisotopic Mass

412.15220 Da

IUPAC Name

4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0^{3,7}]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde

Traditional Name

4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0^{3,7}]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=CC(C(=O)C2=C(O)C=C(C)C3=C2OC2(C)OCC(C)C2C3)=C1C=O

InChI Identifier

InChI=1S/C23H24O7/c1-11-5-18(26)20(21(27)15-6-13(25)7-19(28-4)16(15)9-24)22-14(11)8-17-12(2)10-29-23(17,3)30-22/h5-7,9,12,17,25-26H,8,10H2,1-4H3

InChI Key

CCRDXZGFEZQDRL-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzophenones. These are organic compounds containing a ketone attached to two phenyl groups.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzophenones

Direct Parent

Benzophenones

Alternative Parents

Substituents

Benzophenone
Aryl-phenylketone
1-benzopyran
Methoxyphenol
Benzopyran
Chromane
Hydroxybenzaldehyde
Furopyran
Phenoxy compound
Methoxybenzene
Aryl ketone
Phenol ether
Benzoyl
Benzaldehyde
Anisole
1-hydroxy-2-unsubstituted benzenoid
Ketal
Aryl-aldehyde
Phenol
Alkyl aryl ether
Pyran
Vinylogous acid
Tetrahydrofuran
Furan
Ketone
Oxacycle
Organoheterocyclic compound
Ether
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aldehyde
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	4.54	ChemAxon
pKa (Strongest Acidic)	6.77	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	102.29 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	111.13 m³·mol⁻¹	ChemAxon
Polarizability	42.55 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78444601

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139588526

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde (NP0289601)

MOL for NP0289601 (4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde)

3D MOL for NP0289601 (4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde)

3D SDF for NP0289601 (4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde)

3D-SDF for NP0289601 (4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde)

PDB for NP0289601 (4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde)

3D PDB for NP0289601 (4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde)

SMILES for NP0289601 (4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde)

INCHI for NP0289601 (4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde)

Structure for NP0289601 (4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde)

3D Structure for NP0289601 (4-hydroxy-2-{12-hydroxy-3,6,10-trimethyl-2,4-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),10,12-triene-13-carbonyl}-6-methoxybenzaldehyde)