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 |
|---|---|---|
| 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 Mar |
|
| Microwave-promoted three-component coupling of aldehyde, alkyne, and amine via C-H activation catalyzed by copper in water. | 2004 Mar 18 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:03:32 GMT 2023
by
admin
on
Sat Dec 16 11:03:32 GMT 2023
|
| Record UNII |
2BQC0016L7
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
52183-82-1
Created by
admin on Sat Dec 16 11:03:32 GMT 2023 , Edited by admin on Sat Dec 16 11:03:32 GMT 2023
|
PRIMARY | |||
|
2BQC0016L7
Created by
admin on Sat Dec 16 11:03:32 GMT 2023 , Edited by admin on Sat Dec 16 11:03:32 GMT 2023
|
PRIMARY | |||
|
94239
Created by
admin on Sat Dec 16 11:03:32 GMT 2023 , Edited by admin on Sat Dec 16 11:03:32 GMT 2023
|
PRIMARY | |||
|
257-714-2
Created by
admin on Sat Dec 16 11:03:32 GMT 2023 , Edited by admin on Sat Dec 16 11:03:32 GMT 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ENANTIOMER -> RACEMATE | |||
|
|
ENANTIOMER -> RACEMATE |
