Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H11N3O.2ClH |
| Molecular Weight | 226.104 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.Cl.CNC1=NC(OC)=CC=C1N
InChI
InChIKey=GYLCRBBRGGGHBS-UHFFFAOYSA-N
InChI=1S/C7H11N3O.2ClH/c1-9-7-5(8)3-4-6(10-7)11-2;;/h3-4H,8H2,1-2H3,(H,9,10);2*1H
| Molecular Formula | C7H11N3O |
| Molecular Weight | 153.1817 |
| 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
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:46:47 GMT 2025
by
admin
on
Mon Mar 31 20:46:47 GMT 2025
|
| Record UNII |
200C548F9J
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
83732-72-3
Created by
admin on Mon Mar 31 20:46:47 GMT 2025 , Edited by admin on Mon Mar 31 20:46:47 GMT 2025
|
PRIMARY | |||
|
200C548F9J
Created by
admin on Mon Mar 31 20:46:47 GMT 2025 , Edited by admin on Mon Mar 31 20:46:47 GMT 2025
|
PRIMARY | |||
|
DTXSID80879796
Created by
admin on Mon Mar 31 20:46:47 GMT 2025 , Edited by admin on Mon Mar 31 20:46:47 GMT 2025
|
PRIMARY | |||
|
280-622-9
Created by
admin on Mon Mar 31 20:46:47 GMT 2025 , Edited by admin on Mon Mar 31 20:46:47 GMT 2025
|
PRIMARY | |||
|
5743759
Created by
admin on Mon Mar 31 20:46:47 GMT 2025 , Edited by admin on Mon Mar 31 20:46:47 GMT 2025
|
PRIMARY |