Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H7NO |
| Molecular Weight | 109.1259 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CN=CC=C1
InChI
InChIKey=UMJSCPRVCHMLSP-UHFFFAOYSA-N
InChI=1S/C6H7NO/c1-8-6-3-2-4-7-5-6/h2-5H,1H3
| Molecular Formula | C6H7NO |
| Molecular Weight | 109.1259 |
| 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 |
|---|---|---|
| Development and validation of a specific and sensitive GC-FID method for the determination of impurities in 5-chlorovaleroyl chloride. | 2010-11-02 |
|
| Lead optimization of 4-acetylamino-2-(3,5-dimethylpyrazol-1-yl)-6-pyridylpyrimidines as A2A adenosine receptor antagonists for the treatment of Parkinson's disease. | 2008-11-27 |
|
| Pyridine-catalyzed stereoselective addition of acyclic 1,2-diones to acetylenic esters: synthetic and theoretical studies of an unprecedented rearrangement. | 2008 |
|
| Reactions of sulphate radicals with substituted pyridines: a structure-reactivity correlation analysis. | 2007-12-03 |
|
| Benzyl ether structure-activity relationships in a series of ketopiperazine-based renin inhibitors. | 2005-11-01 |
|
| Characterization of endoperoxide and hydroperoxide intermediates in the reaction of pyridoxine with singlet oxygen. | 2002-10-16 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:02:13 GMT 2025
by
admin
on
Mon Mar 31 19:02:13 GMT 2025
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| Record UNII |
XV2A2D8595
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| Record Status |
Validated (UNII)
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| Record Version |
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