Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H13N |
| Molecular Weight | 111.1848 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(CC=C)CC=C
InChI
InChIKey=WGESLFUSXZBFQF-UHFFFAOYSA-N
InChI=1S/C7H13N/c1-4-6-8(3)7-5-2/h4-5H,1-2,6-7H2,3H3
| Molecular Formula | C7H13N |
| Molecular Weight | 111.1848 |
| 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 |
|---|---|---|
| Secondary and tertiary polydiallylammonium salts: novel polymers with high antimicrobial activity. | 2009-11-09 |
|
| Layer-by-layer assembly of nacre-like nanostructured composites with antimicrobial properties. | 2005-12-06 |
|
| Theoretical study of factors controlling rates of cyclization of radical intermediates from diallylamine and diallylammonium monomers in radical polymerizations. | 2002-07-26 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:55:01 GMT 2025
by
admin
on
Mon Mar 31 19:55:01 GMT 2025
|
| Record UNII |
3479W9P84T
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
2424-01-3
Created by
admin on Mon Mar 31 19:55:01 GMT 2025 , Edited by admin on Mon Mar 31 19:55:01 GMT 2025
|
PRIMARY | |||
|
219-354-4
Created by
admin on Mon Mar 31 19:55:01 GMT 2025 , Edited by admin on Mon Mar 31 19:55:01 GMT 2025
|
PRIMARY | |||
|
75501
Created by
admin on Mon Mar 31 19:55:01 GMT 2025 , Edited by admin on Mon Mar 31 19:55:01 GMT 2025
|
PRIMARY | |||
|
3479W9P84T
Created by
admin on Mon Mar 31 19:55:01 GMT 2025 , Edited by admin on Mon Mar 31 19:55:01 GMT 2025
|
PRIMARY | |||
|
DTXSID2062402
Created by
admin on Mon Mar 31 19:55:01 GMT 2025 , Edited by admin on Mon Mar 31 19:55:01 GMT 2025
|
PRIMARY |