NP-MRD: Showing NP-Card for 1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate (NP0296576)

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Record Information

Version

2.0

Created at

2022-09-10 06:14:12 UTC

Updated at

2022-09-10 06:14:13 UTC

NP-MRD ID

NP0296576

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate

Description

1-Hydroxy-1-[tetrahydro-4-hydroxy-2-(hydroxymethyl)-5-oxofuran-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate belongs to the class of organic compounds known as p-hydroxybenzoic acid alkyl esters. These are aromatic compounds containing a benzoic acid, which is esterified with an alkyl group and para-substituted with a hydroxyl group. Based on a literature review very few articles have been published on 1-hydroxy-1-[tetrahydro-4-hydroxy-2-(hydroxymethyl)-5-oxofuran-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102208142D          

 25 26  0  0  0  0            999 V2000
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    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
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   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
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6224   -1.5787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4429   -1.6649    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8019   -0.1576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.5099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0319    1.2945    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0714    0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7389    0.7399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0714   -0.5701    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
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  2  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  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
 23 25  1  0  0  0  0
 17 25  1  0  0  0  0
M  END

     RDKit          3D

 45 46  0  0  0  0  0  0  0  0999 V2000
    3.9390    0.5437   -1.0671 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5361   -0.4003   -0.0043 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4391   -1.3995    0.3318 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1615   -2.3319    1.3102 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1119   -3.3140    1.6032 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9518   -2.2553    1.9611 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0555   -1.2662    1.6297 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8526   -1.1950    2.2814 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3273   -0.3286    0.6504 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3718    0.7216    0.3014 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6188    1.5727   -0.5877 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1384    0.8350    0.9349 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8215    1.7980    0.6648 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1143    2.7000    1.8515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1383    1.2545    0.1820 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9802    2.3399   -0.0401 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0100    0.3985   -1.0512 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6129    1.1762   -2.2765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7153    0.2755   -3.3627 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3550   -0.2429   -1.3170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3315   -1.5955   -0.6351 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9893   -1.4725    0.5950 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8778   -1.8188   -0.4519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3813   -2.8824    0.0061 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1673   -0.6996   -0.8542 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9503    1.5662   -0.6270 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9307    0.2926   -1.4830 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2422    0.5703   -1.9267 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3837   -1.4442   -0.1896 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7824   -3.0695    2.3254 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7606   -3.0039    2.7278 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6372   -1.8701    2.9982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4326    2.4600   -0.1434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8436    3.4518    1.5049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6013    2.1190    2.6747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1915    3.2092    2.1954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6406    0.6195    0.9543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5094    2.2990   -0.8498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5693    1.5150   -2.2698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3435    1.9693   -2.4847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1370    0.7022   -4.1486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5699   -0.3303   -2.4142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1605    0.3722   -0.8938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8308   -2.3839   -1.1995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8662   -1.9688    0.5937 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 12  1  0
 12 10  1  0
 10 11  2  0
 10  9  1  0
  9  7  2  0
  7  8  1  0
  7  6  1  0
  6  4  2  0
  4  5  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  6
 18 19  1  0
 17 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  2  0
 23 25  1  0
  2  9  1  0
 25 17  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 13 33  1  6
  8 32  1  0
  6 31  1  0
  5 30  1  0
  3 29  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
 15 37  1  1
 16 38  1  0
 18 39  1  0
 18 40  1  0
 19 41  1  0
 20 42  1  0
 20 43  1  0
 21 44  1  6
 22 45  1  0
M  END


  Mrv1652309102208142D          

 25 26  0  0  0  0            999 V2000
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    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
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   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
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6224   -1.5787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4429   -1.6649    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8019   -0.1576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.5099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0319    1.2945    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0714    0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7389    0.7399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0714   -0.5701    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
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  2  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  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
 23 25  1  0  0  0  0
 17 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0296576

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(OC(=O)C1=C(O)C=C(O)C=C1C)C(O)C1(CO)CC(O)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C16H20O9/c1-7-3-9(18)4-10(19)12(7)15(23)24-8(2)13(21)16(6-17)5-11(20)14(22)25-16/h3-4,8,11,13,17-21H,5-6H2,1-2H3

> <INCHI_KEY>
UPELWWMOWRABTA-UHFFFAOYSA-N

> <FORMULA>
C16H20O9

> <MOLECULAR_WEIGHT>
356.327

> <EXACT_MASS>
356.110732224

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
33.7894348125304

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate

> <JCHEM_LOGP>
0.6468538160000008

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.551018390809356

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.698199974510342

> <JCHEM_PKA_STRONGEST_BASIC>
-3.125552157685446

> <JCHEM_POLAR_SURFACE_AREA>
153.74999999999997

> <JCHEM_REFRACTIVITY>
83.1074

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334  -3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -3.850   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -2.667  -4.620   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000  -1.540   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -1.540   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.335  -1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.668  -3.850   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.002  -1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.628  -2.947   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      10.160  -3.108   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.097  -0.294   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.002   0.952   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       7.526   2.416   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.467   0.476   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.713   1.381   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       9.467  -1.064   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7    2   10                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   20   25                                             
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   17                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

View in JSmol

Synonyms

Value	Source
1-Hydroxy-1-[tetrahydro-4-hydroxy-2-(hydroxymethyl)-5-oxofuran-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoic acid	Generator

Chemical Formula

C₁₆H₂₀O₉

Average Mass

356.3270 Da

Monoisotopic Mass

356.11073 Da

IUPAC Name

1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate

Traditional Name

1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate

CAS Registry Number

Not Available

SMILES

CC(OC(=O)C1=C(O)C=C(O)C=C1C)C(O)C1(CO)CC(O)C(=O)O1

InChI Identifier

InChI=1S/C16H20O9/c1-7-3-9(18)4-10(19)12(7)15(23)24-8(2)13(21)16(6-17)5-11(20)14(22)25-16/h3-4,8,11,13,17-21H,5-6H2,1-2H3

InChI Key

UPELWWMOWRABTA-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 p-hydroxybenzoic acid alkyl esters. These are aromatic compounds containing a benzoic acid, which is esterified with an alkyl group and para-substituted with a hydroxyl group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

p-Hydroxybenzoic acid alkyl esters

Alternative Parents

Substituents

P-hydroxybenzoic acid alkyl ester
O-hydroxybenzoic acid ester
Dihydroxybenzoic acid
Salicylic acid or derivatives
Benzoyl
M-cresol
Resorcinol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Toluene
Dicarboxylic acid or derivatives
Gamma butyrolactone
Vinylogous acid
Tetrahydrofuran
Lactone
Carboxylic acid ester
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Primary alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	0.65	ChemAxon
pKa (Strongest Acidic)	8.7	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	153.75 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	83.11 m³·mol⁻¹	ChemAxon
Polarizability	33.79 Å³	ChemAxon
Number of Rings	2	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

78444643

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139584868

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate (NP0296576)

MOL for NP0296576 (1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate)

3D MOL for NP0296576 (1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate)

3D SDF for NP0296576 (1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate)

3D-SDF for NP0296576 (1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate)

PDB for NP0296576 (1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate)

3D PDB for NP0296576 (1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate)

SMILES for NP0296576 (1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate)

INCHI for NP0296576 (1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate)

Structure for NP0296576 (1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate)

3D Structure for NP0296576 (1-hydroxy-1-[4-hydroxy-2-(hydroxymethyl)-5-oxooxolan-2-yl]propan-2-yl 2,4-dihydroxy-6-methylbenzoate)