Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H8N2 |
| Molecular Weight | 84.1197 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=NCCN1
InChI
InChIKey=VWSLLSXLURJCDF-UHFFFAOYSA-N
InChI=1S/C4H8N2/c1-4-5-2-3-6-4/h2-3H2,1H3,(H,5,6)
| Molecular Formula | C4H8N2 |
| Molecular Weight | 84.1197 |
| 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 |
|---|---|---|
| Tandem reactions of 1,3-diacid chlorides with 2-methylimidazoline and 2-methyl-1,4,5,6-tetrahydropyrimidine: one-pot synthesis of 1,8-naphthyridinetetraones. | 2008-07-04 |
|
| Synthesis of heterocyclic compounds via nucleophilic aroylation catalyzed by imidazolidenyl carbene. | 2006-12 |
|
| Unexpected ring expansion of an enantiopure imidazoline carbene ligand. | 2006-07-06 |
|
| Nucleophilic acylation of arylfluorides catalyzed by imidazolidenyl carbene. | 2003-06-07 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:20:11 GMT 2025
by
admin
on
Mon Mar 31 21:20:11 GMT 2025
|
| Record UNII |
987F50E3PE
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
64326
Created by
admin on Mon Mar 31 21:20:11 GMT 2025 , Edited by admin on Mon Mar 31 21:20:11 GMT 2025
|
PRIMARY | |||
|
208-596-6
Created by
admin on Mon Mar 31 21:20:11 GMT 2025 , Edited by admin on Mon Mar 31 21:20:11 GMT 2025
|
PRIMARY | |||
|
Lysidine (chemical)
Created by
admin on Mon Mar 31 21:20:11 GMT 2025 , Edited by admin on Mon Mar 31 21:20:11 GMT 2025
|
PRIMARY | |||
|
534-26-9
Created by
admin on Mon Mar 31 21:20:11 GMT 2025 , Edited by admin on Mon Mar 31 21:20:11 GMT 2025
|
PRIMARY | |||
|
C101421
Created by
admin on Mon Mar 31 21:20:11 GMT 2025 , Edited by admin on Mon Mar 31 21:20:11 GMT 2025
|
PRIMARY | |||
|
DTXSID2060204
Created by
admin on Mon Mar 31 21:20:11 GMT 2025 , Edited by admin on Mon Mar 31 21:20:11 GMT 2025
|
PRIMARY | |||
|
987F50E3PE
Created by
admin on Mon Mar 31 21:20:11 GMT 2025 , Edited by admin on Mon Mar 31 21:20:11 GMT 2025
|
PRIMARY | |||
|
m6966
Created by
admin on Mon Mar 31 21:20:11 GMT 2025 , Edited by admin on Mon Mar 31 21:20:11 GMT 2025
|
PRIMARY | Merck Index | ||
|
10798
Created by
admin on Mon Mar 31 21:20:11 GMT 2025 , Edited by admin on Mon Mar 31 21:20:11 GMT 2025
|
PRIMARY |