Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H15N.BH3 |
| Molecular Weight | 115.025 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
B.CCN(CC)CC
InChI
InChIKey=KDKNBGWKECQREO-UHFFFAOYSA-N
InChI=1S/C6H15N.BH3/c1-4-7(5-2)6-3;/h4-6H2,1-3H3;1H3
| Molecular Formula | BH3 |
| Molecular Weight | 13.835 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C6H15N |
| Molecular Weight | 101.19 |
| 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 |
|---|---|---|
| Acrolein and chloroacetaldehyde: an examination of the cell and cell-free biomarkers of toxicity. | 2013-02-25 |
|
| Omega-3 fatty acid oxidation products prevent vascular endothelial cell activation by coplanar polychlorinated biphenyls. | 2011-02-15 |
|
| Inhibition of DNA cross-linking by mitomycin C by peroxidase-mediated oxidation of mitomycin C hydroquinone. | 2001-09-14 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:43:53 GMT 2025
by
admin
on
Mon Mar 31 23:43:53 GMT 2025
|
| Record UNII |
WEA26VJ71E
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
WEA26VJ71E
Created by
admin on Mon Mar 31 23:43:54 GMT 2025 , Edited by admin on Mon Mar 31 23:43:54 GMT 2025
|
PRIMARY | |||
|
59740
Created by
admin on Mon Mar 31 23:43:54 GMT 2025 , Edited by admin on Mon Mar 31 23:43:54 GMT 2025
|
PRIMARY | |||
|
264094
Created by
admin on Mon Mar 31 23:43:54 GMT 2025 , Edited by admin on Mon Mar 31 23:43:54 GMT 2025
|
PRIMARY | |||
|
DTXSID20938098
Created by
admin on Mon Mar 31 23:43:54 GMT 2025 , Edited by admin on Mon Mar 31 23:43:54 GMT 2025
|
PRIMARY | |||
|
1722-26-5
Created by
admin on Mon Mar 31 23:43:53 GMT 2025 , Edited by admin on Mon Mar 31 23:43:53 GMT 2025
|
PRIMARY |