Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3H2ClN |
| Molecular Weight | 87.508 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC(=C)C#N
InChI
InChIKey=OYUNTGBISCIYPW-UHFFFAOYSA-N
InChI=1S/C3H2ClN/c1-3(4)2-5/h1H2
| Molecular Formula | C3H2ClN |
| Molecular Weight | 87.508 |
| 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 |
|---|---|---|
| Asymmetric conjugate addition of oxindoles to 2-chloroacrylonitrile: a highly effective organocatalytic strategy for simultaneous construction of 1,3-nonadjacent stereocenters leading to chiral pyrroloindolines. | 2010-12-27 |
|
| The nucleophilic reactivity of fluoromethoxycarbene. | 2010-08-06 |
|
| Synthesis of the highly selective p38 MAPK inhibitor UR-13756 for possible therapeutic use in Werner syndrome. | 2010-02 |
|
| Chiral 2-endo-substituted 9-oxabispidines: novel ligands for enantioselective copper(II)-catalyzed Henry reactions. | 2009-11-23 |
|
| Latent nucleophilicity of dichlorocarbene. | 2009-05-07 |
|
| Dual-function cinchona alkaloid catalysis: catalytic asymmetric tandem conjugate addition-protonation for the direct creation of nonadjacent stereocenters. | 2006-03-29 |
|
| A short synthesis of 10-hydroxy 7-spirocyclopropanated camphor. | 2005-09-30 |
|
| Effects of aliphatic nitriles in micromass cultures of rat embryo limb bud cells. | 2004-06 |
|
| A novel bornane synthesis by an old idea. | 2002-05-31 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:12:25 GMT 2025
by
admin
on
Mon Mar 31 19:12:25 GMT 2025
|
| Record UNII |
FFJ1QHD154
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
FFJ1QHD154
Created by
admin on Mon Mar 31 19:12:25 GMT 2025 , Edited by admin on Mon Mar 31 19:12:25 GMT 2025
|
PRIMARY | |||
|
213-055-2
Created by
admin on Mon Mar 31 19:12:25 GMT 2025 , Edited by admin on Mon Mar 31 19:12:25 GMT 2025
|
PRIMARY | |||
|
70198
Created by
admin on Mon Mar 31 19:12:25 GMT 2025 , Edited by admin on Mon Mar 31 19:12:25 GMT 2025
|
PRIMARY | |||
|
DTXSID6052613
Created by
admin on Mon Mar 31 19:12:25 GMT 2025 , Edited by admin on Mon Mar 31 19:12:25 GMT 2025
|
PRIMARY | |||
|
300000052989
Created by
admin on Mon Mar 31 19:12:25 GMT 2025 , Edited by admin on Mon Mar 31 19:12:25 GMT 2025
|
PRIMARY | |||
|
511714
Created by
admin on Mon Mar 31 19:12:25 GMT 2025 , Edited by admin on Mon Mar 31 19:12:25 GMT 2025
|
PRIMARY | |||
|
920-37-6
Created by
admin on Mon Mar 31 19:12:25 GMT 2025 , Edited by admin on Mon Mar 31 19:12:25 GMT 2025
|
PRIMARY |