Details
Stereochemistry | ACHIRAL |
Molecular Formula | C8H7Cl |
Molecular Weight | 138.594 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=CC=C(C=C)C=C1
InChI
InChIKey=KTZVZZJJVJQZHV-UHFFFAOYSA-N
InChI=1S/C8H7Cl/c1-2-7-3-5-8(9)6-4-7/h2-6H,1H2
Molecular Formula | C8H7Cl |
Molecular Weight | 138.594 |
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 |
---|---|---|
Biotransformations catalyzed by cloned p-cymene monooxygenase from Pseudomonas putida F1. | 2001 Apr |
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A cyclodextrin-modified ketoester for stereoselective epoxidation of alkenes. | 2003 Aug 22 |
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Catalytic asymmetric heterogeneous aziridination of styrene derivatives using bis(oxazoline)-modified Cu2+-exchanged zeolite Y. | 2004 Dec 21 |
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Crystal-like pattern formation in polymerization-induced phase separation. | 2004 Oct |
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Synthesis, characterization and olefin/CO exchange reactions of pyrazolylborato complexes of copper(I). | 2006 Aug 7 |
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Manganese-substituted carbonic anhydrase as a new peroxidase. | 2006 Feb 8 |
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Bimetallic effects in homopolymerization of styrene and copolymerization of ethylene and styrenic comonomers: scope, kinetics, and mechanism. | 2008 Feb 20 |
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Heterogeneous allylsilylation of aromatic and aliphatic alkenes catalyzed by proton-exchanged montmorillonite. | 2010 Apr 2 |
|
Structure-toxicity relationship study of para-halogenated styrene analogues in CYP2E1 transgenic cells. | 2012 May 5 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:47:00 GMT 2023
by
admin
on
Sat Dec 16 08:47:00 GMT 2023
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Record UNII |
T0J05U220F
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Record Status |
Validated (UNII)
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Record Version |
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