Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H15NO |
| Molecular Weight | 129.2001 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCC(N)=O
InChI
InChIKey=AEDIXYWIVPYNBI-UHFFFAOYSA-N
InChI=1S/C7H15NO/c1-2-3-4-5-6-7(8)9/h2-6H2,1H3,(H2,8,9)
| Molecular Formula | C7H15NO |
| Molecular Weight | 129.2001 |
| 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 |
|---|---|---|
| DFT-based simulations of IR amide I' spectra for a small protein in solution. Comparison of explicit and empirical solvent models. | 2010-10-14 |
|
| Structural elucidation of an unknown Simvastatin by-product in industrial synthesis starting from Lovastatin. | 2007-11-30 |
|
| Amide and ester derivatives of N3-(4-methoxyfumaroyl)-(S)-2,3-diaminopropanoic acid: the selective inhibitor of glucosamine-6-phosphate synthase. | 2001-04 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:59:16 GMT 2025
by
admin
on
Mon Mar 31 19:59:16 GMT 2025
|
| Record UNII |
6QX6H3415T
|
| 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 |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DB02641
Created by
admin on Mon Mar 31 19:59:16 GMT 2025 , Edited by admin on Mon Mar 31 19:59:16 GMT 2025
|
PRIMARY | |||
|
3819
Created by
admin on Mon Mar 31 19:59:16 GMT 2025 , Edited by admin on Mon Mar 31 19:59:16 GMT 2025
|
PRIMARY | |||
|
6QX6H3415T
Created by
admin on Mon Mar 31 19:59:16 GMT 2025 , Edited by admin on Mon Mar 31 19:59:16 GMT 2025
|
PRIMARY | |||
|
136449
Created by
admin on Mon Mar 31 19:59:16 GMT 2025 , Edited by admin on Mon Mar 31 19:59:16 GMT 2025
|
PRIMARY | |||
|
628-62-6
Created by
admin on Mon Mar 31 19:59:16 GMT 2025 , Edited by admin on Mon Mar 31 19:59:16 GMT 2025
|
PRIMARY | |||
|
DTXSID50211886
Created by
admin on Mon Mar 31 19:59:16 GMT 2025 , Edited by admin on Mon Mar 31 19:59:16 GMT 2025
|
PRIMARY |