Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H13N.ClH |
| Molecular Weight | 147.646 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CN(CC=C)CC=C
InChI
InChIKey=VNLHWLYAOHNSCH-UHFFFAOYSA-N
InChI=1S/C7H13N.ClH/c1-4-6-8(3)7-5-2;/h4-5H,1-2,6-7H2,3H3;1H
| 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 |
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| 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
Tue Apr 01 16:38:36 GMT 2025
by
admin
on
Tue Apr 01 16:38:36 GMT 2025
|
| Record UNII |
59F4RD2HCW
|
| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID20779049
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