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Benzene, [(2,2-dichloro-1-fluoroethenyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56354-46-2

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56354-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56354-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,5 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56354-46:
(7*5)+(6*6)+(5*3)+(4*5)+(3*4)+(2*4)+(1*6)=132
132 % 10 = 2
So 56354-46-2 is a valid CAS Registry Number.

56354-46-2SDS

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 (2,2-dichloro-1-fluoroethenyl)sulfanylbenzene

1.2 Other means of identification

Product number -
Other names 2,2-Dichlor-1-fluorvinyl-phenylsulfid

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:56354-46-2 SDS

56354-46-2Relevant academic research and scientific papers

Synthesis and Diels-Alder cycloaddition reactions of [(2,2-dichloro-1- fluoroethenyl)sulfinyl] benzene and [(2-chloro-1,2-difluoro ethenyl)sulfinyl] benzene

Sridhar, Madabhushi,Leela Krishna,Madhusudana Rao, Jampani

, p. 3539 - 3545 (2007/10/03)

Synthesis of [(2,2-dichloro-1-fluoroethenyl)sulfinyl] benzene and [(2- chloro-1,2-difluoro ethenyl)sulfinyl] benzene and their Dieis-Alder cycloadditions with cyclopentadiene, furan and 1,3-diphenylisobenzofuran under thermal and microwave irradiation conditions are described. 2000 Elsevier Science Ltd.

DISTINCTIVE AND SOLVENT-DEPENDENT BEHAVIOUR OF SOME PER(CHLORO,FLUORO)ETHANES IN THEIR REACTIONS WITH PhSNa. COMPETING MECHAMISTIC PATHWAYS IN HALOPHILIC REACTIONS

Li, Xing-ya,Pan, He-qi,Fu, Wei-min,Jiang, Xi-kui

, p. 213 - 230 (2007/10/02)

Per(chloro,fluoro)ethanes CF2XCCl2Y (1) react spontaneously with PhSNa at room temperature or below to give PhSCF2CCl2Y (2) in fair to good yield, which as well as the by-products PhSCF2CClYH (3) and PhSCF=CCl2 (4) (for 1b and 1c) are most probably produced by an anionic chain process initiated by the chlorophilic attack of PhS- on C-Cl bonds.In case of 1c, the coexistence of two competitive reaction pathways is indicated by the two products 2b and PhSCCl2CF3 (10).The reaction rates and the product distribution have been found to be highly solvent-dependent.Products 2b, 4 and 10 all react further with PhSNa to afford multi-substituted ethylenes PhSCF=C(Cl)SPh (7) (PhS)2C=C(Cl)SPh (8) and (PhS)2C=C(SPh)2 (9).

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