Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | 2ClH.H4N2 |
| Molecular Weight | 104.967 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.Cl.NN
InChI
InChIKey=LIAWOTKNAVAKCX-UHFFFAOYSA-N
InChI=1S/2ClH.H4N2/c;;1-2/h2*1H;1-2H2
| 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 |
| Molecular Formula | H4N2 |
| Molecular Weight | 32.0452 |
| 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 |
|---|---|---|
| Molecular mechanism of anaerobic ammonium oxidation. | 2011-10-02 |
|
| Small-molecule activators of AMP-activated protein kinase (AMPK), RSVA314 and RSVA405, inhibit adipogenesis. | 2011-04-29 |
|
| Carbamoylating chemoresistance induced by cobalt pretreatment in C6 glioma cells: putative roles of hypoxia-inducible factor-1. | 2004-03 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:56:39 GMT 2025
by
admin
on
Mon Mar 31 19:56:39 GMT 2025
|
| Record UNII |
KM8DD9J0C8
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
Hydrazine dihydrochloride
Created by
admin on Mon Mar 31 19:56:39 GMT 2025 , Edited by admin on Mon Mar 31 19:56:39 GMT 2025
|
PRIMARY | |||
|
m6079
Created by
admin on Mon Mar 31 19:56:39 GMT 2025 , Edited by admin on Mon Mar 31 19:56:39 GMT 2025
|
PRIMARY | Merck Index | ||
|
KM8DD9J0C8
Created by
admin on Mon Mar 31 19:56:39 GMT 2025 , Edited by admin on Mon Mar 31 19:56:39 GMT 2025
|
PRIMARY | |||
|
300000053414
Created by
admin on Mon Mar 31 19:56:39 GMT 2025 , Edited by admin on Mon Mar 31 19:56:39 GMT 2025
|
PRIMARY | |||
|
5341-61-7
Created by
admin on Mon Mar 31 19:56:39 GMT 2025 , Edited by admin on Mon Mar 31 19:56:39 GMT 2025
|
PRIMARY | |||
|
226-283-2
Created by
admin on Mon Mar 31 19:56:39 GMT 2025 , Edited by admin on Mon Mar 31 19:56:39 GMT 2025
|
PRIMARY | |||
|
C029424
Created by
admin on Mon Mar 31 19:56:39 GMT 2025 , Edited by admin on Mon Mar 31 19:56:39 GMT 2025
|
PRIMARY | |||
|
17548
Created by
admin on Mon Mar 31 19:56:39 GMT 2025 , Edited by admin on Mon Mar 31 19:56:39 GMT 2025
|
PRIMARY | |||
|
14011-37-1
Created by
admin on Mon Mar 31 19:56:39 GMT 2025 , Edited by admin on Mon Mar 31 19:56:39 GMT 2025
|
NON-SPECIFIC STOICHIOMETRY | |||
|
DTXSID9063798
Created by
admin on Mon Mar 31 19:56:39 GMT 2025 , Edited by admin on Mon Mar 31 19:56:39 GMT 2025
|
PRIMARY | |||
|
2122
Created by
admin on Mon Mar 31 19:56:39 GMT 2025 , Edited by admin on Mon Mar 31 19:56:39 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
PARENT -> SALT/SOLVATE |
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
|