Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C11H8O3 |
| Molecular Weight | 188.1794 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CC2=C(C=C1)C=C(O)C=C2
InChI
InChIKey=KAUQJMHLAFIZDU-UHFFFAOYSA-N
InChI=1S/C11H8O3/c12-10-4-3-7-5-9(11(13)14)2-1-8(7)6-10/h1-6,12H,(H,13,14)
| Molecular Formula | C11H8O3 |
| Molecular Weight | 188.1794 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Co-crystals of caffeine and hydroxy-2-naphthoic acids: unusual formation of the carboxylic acid dimer in the presence of a heterosynthon. | 2007-05-11 |
|
| Addendum to Food Additives and Contaminants 2002, 19, 492-501 migration of monomers from liquid crystalline poly(p-hydroxybenzoic acid-co-2-hydroxy-6-naphthoic acid). | 2003-03 |
|
| Migration of monomers from liquid crystalline poly(p-hydroxybenzoic acid-co-2-hydroxy-6-naphthoic acid). | 2002-05 |
|
| Induction of 4-hydroxycinnamate decarboxylase in Klebsiella oxytoca cells exposed to substrates and non-substrate 4-hydroxycinnamate analogs. | 2001-12 |
|
| Arylamide inhibitors of HIV-1 integrase. | 1997-04-11 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:34:58 GMT 2025
by
admin
on
Mon Mar 31 19:34:58 GMT 2025
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| Record UNII |
72XA858I6P
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| Record Status |
Validated (UNII)
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| Record Version |
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