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
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Characterization of endoperoxide and hydroperoxide intermediates in the reaction of pyridoxine with singlet oxygen. | 2002 Oct 16 |
|
| Benzyl ether structure-activity relationships in a series of ketopiperazine-based renin inhibitors. | 2005 Nov 1 |
|
| Reactions of sulphate radicals with substituted pyridines: a structure-reactivity correlation analysis. | 2007 Dec 3 |
|
| Pyridine-catalyzed stereoselective addition of acyclic 1,2-diones to acetylenic esters: synthetic and theoretical studies of an unprecedented rearrangement. | 2008 |
|
| 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 Nov 27 |
|
| Development and validation of a specific and sensitive GC-FID method for the determination of impurities in 5-chlorovaleroyl chloride. | 2010 Nov 2 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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DTXSID60223238
Created by
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XV2A2D8595
Created by
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7295-76-3
Created by
admin on Fri Dec 15 18:05:19 GMT 2023 , Edited by admin on Fri Dec 15 18:05:19 GMT 2023
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230-730-7
Created by
admin on Fri Dec 15 18:05:19 GMT 2023 , Edited by admin on Fri Dec 15 18:05:19 GMT 2023
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23719
Created by
admin on Fri Dec 15 18:05:19 GMT 2023 , Edited by admin on Fri Dec 15 18:05:19 GMT 2023
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SUBSTANCE RECORD
