NP-MRD: Showing NP-Card for 3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde (NP0209861)

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Record Information

Version

2.0

Created at

2022-09-05 07:26:49 UTC

Updated at

2022-09-05 07:26:49 UTC

NP-MRD ID

NP0209861

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde

Description

3-Chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde belongs to the class of organic compounds known as hydroxybenzaldehydes. These are organic aromatic compounds containing a benzene ring carrying an aldehyde group and a hydroxyl group. 3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde is found in Neonectria coccinea and Neonectria ditissima. 3-Chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171503072D          

 28 29  0  0  0  0            999 V2000
    5.1113   -3.3288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3969   -3.7413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3969   -4.5663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6824   -4.9788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9679   -4.5663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2534   -4.9788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9679   -3.7413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2534   -3.3288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6824   -3.3288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2951   -2.6004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0697   -2.6004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8942   -2.5716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2815   -1.8431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1060   -1.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4933   -1.0859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3178   -1.0571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7051   -0.3287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2679    0.3710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5296   -0.2999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9169    0.4285    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    8.9668   -0.9995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7913   -0.9707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5795   -1.7280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0167   -2.4276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6294   -3.1560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7550   -1.7568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3677   -2.4852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8443   -1.1435    0.0000 C   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  2  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  4  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 23 26  2  0  0  0  0
 16 26  1  0  0  0  0
 26 27  1  0  0  0  0
 13 28  1  0  0  0  0
M  END

     RDKit          3D

 59 60  0  0  0  0  0  0  0  0999 V2000
   -0.2129   -1.8604    1.3088 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2712   -0.8815    0.2969 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4386   -1.2122   -0.2578 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2170   -0.4550   -1.2457 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6118   -0.2212   -0.7722 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5254   -1.2773   -0.7861 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0473   -2.5131   -1.2472 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8326   -1.1294   -0.3719 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9429   -2.4810   -0.4067 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    6.2777    0.1010    0.0780 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6812    0.3130    0.5356 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3795    1.1387    0.0916 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8168    2.4323    0.5541 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0206    3.3959    0.5764 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0445    0.9934   -0.3301 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2068    2.0941   -0.2841 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4145    0.3512   -0.0359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7254    0.3737   -0.6721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0002   -0.0643   -0.0879 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0964   -1.5687   -0.0314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0350    0.2728   -1.2396 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1507    1.7296   -1.4633 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3034   -0.3997   -0.8942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8860   -1.0500   -1.7204 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7795   -0.2138    0.4991 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9772    0.8658    1.1975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4820    0.6509    1.1183 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0038    0.1681    2.4491 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8347   -1.4056    2.0669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6855   -2.7597    0.8653 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6907   -2.2884    1.8675 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9214   -2.1771    0.0353 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3154   -1.0874   -2.1987 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8229    0.4834   -1.5923 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6681   -3.2917   -1.2726 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6390    0.5013    1.6230 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0547    1.2103    0.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3011   -0.5824    0.3001 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8226    2.5942    0.8854 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2664    2.1614   -0.5429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3959    1.0402    0.8949 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2690    0.9617   -0.7148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9069    1.4177   -1.1338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6137   -0.2233   -1.6676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0464   -1.9648   -0.4675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2941   -1.9688   -0.6832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0190   -2.0175    0.9497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5768   -0.2084   -2.1248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6358    2.3895   -0.7716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2506    1.9810   -1.5552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7492    2.0067   -2.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8348    0.1302    0.5003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7733   -1.1752    1.0708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3010    1.8592    0.8367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2775    0.8310    2.2651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0647    1.7091    1.0305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6664    0.6362    3.2450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1004   -0.9034    2.6102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9916    0.5877    2.7143 H   0  0  0  0  0  0  0  0  0  0  0  0
 28 27  1  0
 27 26  1  0
 26 25  1  0
 25 23  1  0
 23 24  2  0
 23 21  1  0
 21 22  1  0
 21 19  1  0
 19 20  1  1
 19 18  1  0
 18 17  1  0
 17  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 12 15  2  0
 15 16  1  0
 19 27  1  0
 15  5  1  0
 28 57  1  0
 28 58  1  0
 28 59  1  0
 27 56  1  6
 26 54  1  0
 26 55  1  0
 25 52  1  0
 25 53  1  0
 21 48  1  6
 22 49  1  0
 22 50  1  0
 22 51  1  0
 20 45  1  0
 20 46  1  0
 20 47  1  0
 18 43  1  0
 18 44  1  0
 17 41  1  0
 17 42  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  4 33  1  0
  4 34  1  0
  7 35  1  0
 11 36  1  0
 11 37  1  0
 11 38  1  0
 13 39  1  0
 16 40  1  0
M  END


  Mrv1533004171503072D          

 28 29  0  0  0  0            999 V2000
    5.1113   -3.3288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3969   -3.7413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3969   -4.5663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6824   -4.9788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9679   -4.5663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2534   -4.9788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9679   -3.7413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2534   -3.3288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6824   -3.3288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2951   -2.6004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0697   -2.6004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8942   -2.5716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2815   -1.8431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1060   -1.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4933   -1.0859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3178   -1.0571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7051   -0.3287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2679    0.3710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5296   -0.2999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9169    0.4285    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    8.9668   -0.9995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7913   -0.9707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5795   -1.7280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0167   -2.4276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6294   -3.1560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7550   -1.7568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3677   -2.4852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8443   -1.1435    0.0000 C   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  2  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  4  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 23 26  2  0  0  0  0
 16 26  1  0  0  0  0
 26 27  1  0  0  0  0
 13 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0209861

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CCC(=O)C(C)C1(C)CCC(C)=CCC1=C(O)C(Cl)=C(C)C(C=O)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C23H31ClO4/c1-13(10-11-23(5)14(2)7-9-19(26)16(23)4)6-8-17-21(27)18(12-25)15(3)20(24)22(17)28/h6,12,14,16,27-28H,7-11H2,1-5H3

> <INCHI_KEY>
IJEHYEVNWOYGMS-UHFFFAOYSA-N

> <FORMULA>
C23H31ClO4

> <MOLECULAR_WEIGHT>
406.95

> <EXACT_MASS>
406.1910872

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
43.85978536799784

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde

> <ALOGPS_LOGP>
5.61

> <JCHEM_LOGP>
7.016190535333333

> <ALOGPS_LOGS>
-5.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.527539774872622

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.8411996716883285

> <JCHEM_PKA_STRONGEST_BASIC>
-6.043423732795934

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
115.28459999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.10e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       9.541  -6.214   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.207  -6.984   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.207  -8.524   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.874  -9.294   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.540  -8.524   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.206  -9.294   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.540  -6.984   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.206  -6.214   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.874  -6.214   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.151  -4.854   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.597  -4.854   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.136  -4.800   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.859  -3.441   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.398  -3.387   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.121  -2.027   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.660  -1.973   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.383  -0.614   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      13.567   0.692   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      15.922  -0.560   0.000  0.00  0.00           C+0
HETATM   20 Cl   UNK     0      16.645   0.800   0.000  0.00  0.00          Cl+0
HETATM   21  C   UNK     0      16.738  -1.866   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      18.277  -1.812   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      16.015  -3.226   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      16.831  -4.532   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      16.108  -5.891   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      14.476  -3.279   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      13.753  -4.639   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       9.043  -2.135   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7    2   10   11                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   28                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   26                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   16   27                                                  
CONECT   27   26                                                            
CONECT   28   13                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₁ClO₄

Average Mass

406.9500 Da

Monoisotopic Mass

406.19109 Da

IUPAC Name

3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde

Traditional Name

3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde

CAS Registry Number

Not Available

SMILES

CC1CCC(=O)C(C)C1(C)CCC(C)=CCC1=C(O)C(Cl)=C(C)C(C=O)=C1O

InChI Identifier

InChI=1S/C23H31ClO4/c1-13(10-11-23(5)14(2)7-9-19(26)16(23)4)6-8-17-21(27)18(12-25)15(3)20(24)22(17)28/h6,12,14,16,27-28H,7-11H2,1-5H3

InChI Key

IJEHYEVNWOYGMS-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

Species Name	Source	Reference
Neonectria coccinea	LOTUS Database	35616633
Neonectria ditissima	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxybenzaldehydes. These are organic aromatic compounds containing a benzene ring carrying an aldehyde group and a hydroxyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Hydroxybenzaldehydes

Alternative Parents

Substituents

Hydroxybenzaldehyde
4-halophenol
2-halophenol
M-cresol
2-chlorophenol
Benzoyl
4-chlorophenol
Resorcinol
Halobenzene
Chlorobenzene
Toluene
Phenol
Benzenoid
Aryl halide
Monocyclic benzene moiety
Aryl chloride
Vinylogous acid
Cyclic ketone
Ketone
Organochloride
Hydrocarbon derivative
Organohalogen compound
Organic oxide
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	5.61	ALOGPS
logP	7.02	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	5.84	ChemAxon
pKa (Strongest Basic)	-6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	115.28 m³·mol⁻¹	ChemAxon
Polarizability	43.86 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

74177081

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde (NP0209861)

MOL for NP0209861 (3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde)

3D MOL for NP0209861 (3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde)

3D SDF for NP0209861 (3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde)

3D-SDF for NP0209861 (3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde)

PDB for NP0209861 (3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde)

3D PDB for NP0209861 (3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde)

SMILES for NP0209861 (3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde)

INCHI for NP0209861 (3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde)

Structure for NP0209861 (3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde)

3D Structure for NP0209861 (3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-5-(1,2,6-trimethyl-3-oxocyclohexyl)pent-2-en-1-yl]benzaldehyde)