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3-(2,5-DICHLOROPHENYL)-1-PROPENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93794-95-7

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93794-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93794-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,9 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93794-95:
(7*9)+(6*3)+(5*7)+(4*9)+(3*4)+(2*9)+(1*5)=187
187 % 10 = 7
So 93794-95-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H8Cl2/c1-2-3-7-6-8(10)4-5-9(7)11/h2,4-6H,1,3H2

93794-95-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dichloro-2-prop-2-enylbenzene

1.2 Other means of identification

Product number -
Other names 3-(2,5-DICHLOROPHENYL)-1-PROPENE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:93794-95-7 SDS

93794-95-7Downstream Products

93794-95-7Relevant academic research and scientific papers

An Unusually Lower Barrier to Reductive Elimination of an 18-Electron μ3-Allyl(organo)nickel(II) Complex Than Those of a 16-Electron μ3-Allyl Counterpart and a 16-Electron μ1-Allyl Isomer

Kurosawa, Hideo,Ohnishi, Hiroaki,Emoto, Mitsuhiro,Kawasaki, Yoshikane,Murai, Shinji

, p. 6272 - 6273 (2007/10/02)

We report a novel finding that the coupling of allyl and aryl groups on Ni is much more facile in an μ3-allyl form with 18-electron configuration than in both a 16-electron μ3-allyl counterpart and a 16-electron μ1-allyl isomer.This trend seems of particular relevance to the origin of some unique ligand and metal effects upon reactivity and selectivity in catalyses.

Acceleration of the Reductive Elimination Step in Pd-Catalysed Allylic Alkylation by Allylic Substrates

Kurosawa, Hideo,Emoto, Mitsuhiro,Urabe, Akira

, p. 968 - 969 (2007/10/02)

Allylic electrophiles used in Pd-catalysed allylic alkylation greatly accelerate reductive elimination of η3-allyl(organo)palladium(II) complexes, via a PdIV intermediate, to give the coupling products and η3-allylpalladium(II) salts.

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