Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H7NO2 |
| Molecular Weight | 137.136 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)C1=CC=C(O)C=C1
InChI
InChIKey=QXSAKPUBHTZHKW-UHFFFAOYSA-N
InChI=1S/C7H7NO2/c8-7(10)5-1-3-6(9)4-2-5/h1-4,9H,(H2,8,10)
| Molecular Formula | C7H7NO2 |
| Molecular Weight | 137.136 |
| 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 |
|---|---|---|
| Energetics of the O-H bond and of intramolecular hydrogen bonding in HOC6H4C(O)Y (Y = H, CH3, CH2CH=CH2, C[triple bond]CH, CH2F, NH2, NHCH3, NO2, OH, OCH3, OCN, CN, F, Cl, SH, and SCH3) compounds. | 2008-10-09 |
|
| Metabolism of CJ-036878, N-(3-phenethoxybenzyl)-4-hydroxybenzamide, in liver microsomes and recombinant cytochrome P450 enzymes: metabolite identification by LC-UV/MS(n) and (1)H-NMR. | 2007-12 |
|
| CYP3A4 and CYP3A5 catalyse the conversion of the N-methyl-D-aspartate (NMDA) antagonist CJ-036878 to two novel dimers. | 2007-12 |
|
| Amide-N-oxide heterosynthon and amide dimer homosynthon in cocrystals of carboxamide drugs and pyridine N-oxides. | 2007-05-15 |
|
| Metabolic profiling of root exudates of Arabidopsis thaliana. | 2003-04-23 |
|
| Thiazole and thiadiazole analogues as a novel class of adenosine receptor antagonists. | 2001-03-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:39:01 GMT 2025
by
admin
on
Mon Mar 31 19:39:01 GMT 2025
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| Record UNII |
9OU5YD093J
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| Record Status |
Validated (UNII)
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| Record Version |
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9OU5YD093J
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