Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H9NO2 |
| Molecular Weight | 151.1626 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)CC1=CC=C(O)C=C1
InChI
InChIKey=YBPAYPRLUDCSEY-UHFFFAOYSA-N
InChI=1S/C8H9NO2/c9-8(11)5-6-1-3-7(10)4-2-6/h1-4,10H,5H2,(H2,9,11)
| Molecular Formula | C8H9NO2 |
| Molecular Weight | 151.1626 |
| 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 |
|---|---|---|
| Natural product-based phenols as novel probes for mycobacterial and fungal carbonic anhydrases. | 2011-03-24 |
|
| Non-invasive characterization of mouse embryonic stem cell derived cardiomyocytes based on the intensity variation in digital beating video. | 2010-07 |
|
| Unusual products of the aqueous chlorination of atenolol. | 2009-02 |
|
| Host plant-dependent metabolism of 4-hydroxybenzylglucosinolate in Pieris rapae: substrate specificity and effects of genetic modification and plant nitrile hydratase. | 2007-11 |
|
| Pharacine, a natural p-cyclophane and other indole derivatives from Cytophaga sp. strain AM13.1. | 2002-11 |
|
| Structural criteria for the rational design of selective ligands. 3. Quantitative structure-stability relationship for iron(III) complexation by tris-catecholamide siderophores. | 2001-07-30 |
|
| p-Hydroxyphenylacetate decarboxylase from Clostridium difficile. A novel glycyl radical enzyme catalysing the formation of p-cresol. | 2001-03 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:54:57 GMT 2025
by
admin
on
Mon Mar 31 18:54:57 GMT 2025
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| Record UNII |
0HY0N4ITN4
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID4066171
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241-235-0
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86986
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17194-82-0
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| Related Record | Type | Details | ||
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PARENT -> IMPURITY |
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