NP-MRD: Showing NP-Card for (2r)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2e)-2-methylbut-2-enoate (NP0250387)

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Record Information

Version

2.0

Created at

2022-09-07 13:11:52 UTC

Updated at

2022-09-07 13:11:52 UTC

NP-MRD ID

NP0250387

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2e)-2-methylbut-2-enoate

Description

(2R)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2E)-2-methylbut-2-enoate belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. Based on a literature review very few articles have been published on (2R)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2E)-2-methylbut-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072215112D          

 25 25  0  0  1  0            999 V2000
   -1.4289    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1105    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.3480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    0.6336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  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
  9  8  1  6  0  0  0
  9 10  1  1  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  1  0  0  0  0
 13 15  2  0  0  0  0
  9 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END

     RDKit          3D

 49 49  0  0  0  0  0  0  0  0999 V2000
    6.4238   -0.4951    1.3746 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0156   -0.0422    1.4196 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3490    0.0504    0.2957 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9868   -0.2886   -0.9847 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9345    0.5031    0.3204 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4114    0.7878    1.4327 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1935    0.6191   -0.8068 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8908    1.0061   -0.9719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1761    0.1056   -0.3616 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0525    0.1214    1.0652 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1064   -1.2944   -0.7407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7582   -2.2333   -0.1080 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5858   -3.5773   -0.3887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4101   -4.6527    0.1963 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3303   -3.9172   -1.1940 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4883    0.6607   -0.5829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1882    1.1454    0.5374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4293    1.7354    0.4578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1020    2.2069    1.5770 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4724    2.0659    2.8304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0436    1.8732   -0.7640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3840    2.5124   -0.8422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3942    1.4137   -1.8710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1094    0.8020   -1.7882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5431    0.3699   -2.9371 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1539    0.3195    1.3715 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6384   -1.1274    0.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5606   -1.1852    2.2467 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5950    0.1951    2.3931 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0493   -1.3774   -1.0855 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9836    0.1721   -1.1187 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3630    0.0662   -1.8521 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6942    1.2082   -2.0364 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7120    2.0554   -0.5070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4968   -0.6086    1.4422 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3358   -1.5201   -1.7825 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1120   -1.5253   -0.2261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5510   -5.4278   -0.5871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4456   -4.2966    0.4431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9280   -5.1505    1.0617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7596    1.0671    1.5252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4999    2.6232    2.8530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0814    2.4898    3.6545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3049    1.0057    3.0700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3004    3.6299   -0.8282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9573    2.2277    0.0623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9201    2.2574   -1.7795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8377    1.5012   -2.8436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7246   -0.0780   -3.1126 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19 18  1  0
 18 21  2  0
 21 22  1  0
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 23 24  2  0
 24 25  1  0
 24 16  1  0
 16 17  2  0
 16  9  1  0
  9 10  1  1
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
  9  8  1  0
  8  7  1  0
  7  5  1  0
  5  6  2  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
  2  1  1  0
 17 18  1  0
 20 42  1  0
 20 43  1  0
 20 44  1  0
 22 45  1  0
 22 46  1  0
 22 47  1  0
 23 48  1  0
 25 49  1  0
 17 41  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 14 38  1  0
 14 39  1  0
 14 40  1  0
  8 33  1  0
  8 34  1  0
  4 30  1  0
  4 31  1  0
  4 32  1  0
  2 29  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
M  END


  Mrv1652309072215112D          

 25 25  0  0  1  0            999 V2000
   -1.4289    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1105    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.3480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    0.6336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  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
  9  8  1  6  0  0  0
  9 10  1  1  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  1  0  0  0  0
 13 15  2  0  0  0  0
  9 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0250387

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(C)C=C(O)C(=C1)[C@@](O)(COC(C)=O)COC(=O)C(\C)=C\C

> <INCHI_IDENTIFIER>
InChI=1S/C18H24O7/c1-6-11(2)17(21)25-10-18(22,9-24-13(4)19)14-8-16(23-5)12(3)7-15(14)20/h6-8,20,22H,9-10H2,1-5H3/b11-6+/t18-/m1/s1

> <INCHI_KEY>
WGZDBWFXPAKPNU-PMQIGOLDSA-N

> <FORMULA>
C18H24O7

> <MOLECULAR_WEIGHT>
352.383

> <EXACT_MASS>
352.152203113

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
36.39764876020997

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2E)-2-methylbut-2-enoate

> <JCHEM_LOGP>
2.515475255333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.560934002987707

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.352372939374558

> <JCHEM_PKA_STRONGEST_BASIC>
-3.981885744312895

> <JCHEM_POLAR_SURFACE_AREA>
102.29000000000002

> <JCHEM_REFRACTIVITY>
91.48489999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2E)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.667  10.780   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  10.010   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334   8.470   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667   7.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   7.700   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.334   8.470   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       0.000   6.160   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.334   5.390   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.206   3.850   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.874   3.850   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.644   2.516   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.184   2.516   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.954   1.183   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.954   3.850   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11   16                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16    9   17   24                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   16   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   50    0
END

View in JSmol

Synonyms

Value	Source
(2R)-3-(Acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2E)-2-methylbut-2-enoic acid	Generator

Chemical Formula

C₁₈H₂₄O₇

Average Mass

352.3830 Da

Monoisotopic Mass

352.15220 Da

IUPAC Name

(2R)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2E)-2-methylbut-2-enoate

Traditional Name

(2R)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2E)-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

COC1=C(C)C=C(O)C(=C1)[C@@](O)(COC(C)=O)COC(=O)C(\C)=C\C

InChI Identifier

InChI=1S/C18H24O7/c1-6-11(2)17(21)25-10-18(22,9-24-13(4)19)14-8-16(23-5)12(3)7-15(14)20/h6-8,20,22H,9-10H2,1-5H3/b11-6+/t18-/m1/s1

InChI Key

WGZDBWFXPAKPNU-PMQIGOLDSA-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 methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Methoxyphenol
4-alkoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
M-cresol
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Fatty acid ester
Glycerolipid
Toluene
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Carboxylic acid ester
Ether
Carboxylic acid derivative
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Alcohol
Aromatic alcohol
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	2.52	ChemAxon
pKa (Strongest Acidic)	10.35	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	102.29 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	91.48 m³·mol⁻¹	ChemAxon
Polarizability	36.4 Å³	ChemAxon
Number of Rings	1	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

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

163189996

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2e)-2-methylbut-2-enoate (NP0250387)

MOL for NP0250387 ((2r)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2e)-2-methylbut-2-enoate)

3D MOL for NP0250387 ((2r)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2e)-2-methylbut-2-enoate)

3D SDF for NP0250387 ((2r)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2e)-2-methylbut-2-enoate)

3D-SDF for NP0250387 ((2r)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2e)-2-methylbut-2-enoate)

PDB for NP0250387 ((2r)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2e)-2-methylbut-2-enoate)

3D PDB for NP0250387 ((2r)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2e)-2-methylbut-2-enoate)

SMILES for NP0250387 ((2r)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2e)-2-methylbut-2-enoate)

INCHI for NP0250387 ((2r)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2e)-2-methylbut-2-enoate)

Structure for NP0250387 ((2r)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2e)-2-methylbut-2-enoate)

3D Structure for NP0250387 ((2r)-3-(acetyloxy)-2-hydroxy-2-(2-hydroxy-5-methoxy-4-methylphenyl)propyl (2e)-2-methylbut-2-enoate)