Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H11NO |
| Molecular Weight | 101.1469 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(C)NC=O
InChI
InChIKey=SDLAKRCBYGZJRW-UHFFFAOYSA-N
InChI=1S/C5H11NO/c1-5(2,3)6-4-7/h4H,1-3H3,(H,6,7)
| Molecular Formula | C5H11NO |
| Molecular Weight | 101.1469 |
| 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 |
|---|---|---|
| Induction of cytotoxicity, apoptosis and cell cycle arrest by 1-t-butyl carbamoyl, 7-methyl-indole-3-ethyl isothiocyanate (NB7M) in nervous system cancer cells. | 2009-02-06 |
|
| Di-tert-butyl N,N'-(octa-hydro-penta-lene-2,5-di-yl)dicarbamate. | 2008-05-24 |
|
| Solvation properties of N-substituted cis and trans amides are not identical: significant enthalpy and entropy changes are revealed by the use of variable temperature 1H NMR in aqueous and chloroform solutions and ab initio calculations. | 2005-12-29 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:22:51 GMT 2025
by
admin
on
Mon Mar 31 22:22:51 GMT 2025
|
| Record UNII |
GZ0P5X0IRF
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID2062408
Created by
admin on Mon Mar 31 22:22:51 GMT 2025 , Edited by admin on Mon Mar 31 22:22:51 GMT 2025
|
PRIMARY | |||
|
7082
Created by
admin on Mon Mar 31 22:22:51 GMT 2025 , Edited by admin on Mon Mar 31 22:22:51 GMT 2025
|
PRIMARY | |||
|
17045
Created by
admin on Mon Mar 31 22:22:51 GMT 2025 , Edited by admin on Mon Mar 31 22:22:51 GMT 2025
|
PRIMARY | |||
|
GZ0P5X0IRF
Created by
admin on Mon Mar 31 22:22:51 GMT 2025 , Edited by admin on Mon Mar 31 22:22:51 GMT 2025
|
PRIMARY | |||
|
2425-74-3
Created by
admin on Mon Mar 31 22:22:51 GMT 2025 , Edited by admin on Mon Mar 31 22:22:51 GMT 2025
|
PRIMARY | |||
|
5877
Created by
admin on Mon Mar 31 22:22:51 GMT 2025 , Edited by admin on Mon Mar 31 22:22:51 GMT 2025
|
PRIMARY | |||
|
219-369-6
Created by
admin on Mon Mar 31 22:22:51 GMT 2025 , Edited by admin on Mon Mar 31 22:22:51 GMT 2025
|
PRIMARY |