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 |
|---|---|---|
| A novel bornane synthesis by an old idea. | 2002 May 31 |
|
| Effects of aliphatic nitriles in micromass cultures of rat embryo limb bud cells. | 2004 Jun |
|
| A short synthesis of 10-hydroxy 7-spirocyclopropanated camphor. | 2005 Sep 30 |
|
| Dual-function cinchona alkaloid catalysis: catalytic asymmetric tandem conjugate addition-protonation for the direct creation of nonadjacent stereocenters. | 2006 Mar 29 |
|
| Latent nucleophilicity of dichlorocarbene. | 2009 May 7 |
|
| Chiral 2-endo-substituted 9-oxabispidines: novel ligands for enantioselective copper(II)-catalyzed Henry reactions. | 2009 Nov 23 |
|
| The nucleophilic reactivity of fluoromethoxycarbene. | 2010 Aug 6 |
|
| 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 Dec 27 |
|
| Synthesis of the highly selective p38 MAPK inhibitor UR-13756 for possible therapeutic use in Werner syndrome. | 2010 Feb |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:25:52 GMT 2023
by
admin
on
Fri Dec 15 18:25:52 GMT 2023
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| Record UNII |
FFJ1QHD154
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| Record Status |
Validated (UNII)
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| Record Version |
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