Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C6H11NO2 |
| Molecular Weight | 129.157 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)C1CCCN1
InChI
InChIKey=BLWYXBNNBYXPPL-UHFFFAOYSA-N
InChI=1S/C6H11NO2/c1-9-6(8)5-3-2-4-7-5/h5,7H,2-4H2,1H3
| Molecular Formula | C6H11NO2 |
| Molecular Weight | 129.157 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Microwave-promoted three-component coupling of aldehyde, alkyne, and amine via C-H activation catalyzed by copper in water. | 2004-03-18 |
|
| The diastereoisomers methyl 5-(S)-[2-(R)/(S)-methoxycarbonyl)-2,3,4,5-tetrahydropyrrol-1-ylcarbonyl]-1-(4-methylphenyl)-4,5-dihydropyrazole-3-carboxylate. | 2002-03 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:36:19 GMT 2025
by
admin
on
Mon Mar 31 23:36:19 GMT 2025
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| Record UNII |
2BQC0016L7
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| Record Status |
Validated (UNII)
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| Record Version |
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52183-82-1
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2BQC0016L7
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94239
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257-714-2
Created by
admin on Mon Mar 31 23:36:19 GMT 2025 , Edited by admin on Mon Mar 31 23:36:19 GMT 2025
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| Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
