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Benzene, (2-chloro-1-methylethenyl)-, also known as 2-chloro-1-methylvinylbenzene or α-chloro-p-xylene, is an organic compound with the chemical formula C8H9Cl. It is a colorless liquid with a pungent odor and is derived from benzene by substituting one hydrogen atom with a 2-chloro-1-methylethenyl group. Benzene, (2-chloro-1-methylethenyl)- is used as an intermediate in the synthesis of various chemicals, including pharmaceuticals and agrochemicals. It is also employed in the production of polymers and resins. Due to its reactivity and potential health risks, it is important to handle this chemical with proper safety measures.

3360-55-2

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3360-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3360-55-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,6 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3360-55:
(6*3)+(5*3)+(4*6)+(3*0)+(2*5)+(1*5)=72
72 % 10 = 2
So 3360-55-2 is a valid CAS Registry Number.

3360-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name β-chloro-α-methylstyrene

1.2 Other means of identification

Product number -
Other names β-Chlor-α-methyl-styrol

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:3360-55-2 SDS

3360-55-2Relevant academic research and scientific papers

Halofluorination of alkenes using trihaloisocyanuric acids and HF-pyridine

Crespo, Livia T. C.,Ribeiro, Rodrigo Da S.,De Mattos, Marcio C. S.,Esteves, Pierre M.

experimental part, p. 2379 - 2382 (2010/09/04)

Halofluorination of alkenes with a new system (trihaloisocyanuric acids and HF-pyridine) results in the formation of vicinal halofluoroalkanes. The reaction is regioselective leading to Markovnikov-oriented products and the halofluorinated adducts follow anti-addition in the case of cyclohexene and 1-methylcyclohexene. Reaction yields range from 67-88%. Georg Thieme Verlag Stuttgart · New York.

Novel dimerization, alkoxylation, and sulfidation of olefins catalyzed by RuCl3·nH2O

Higashimura, Mitsuteru,Imamura, Keita,Yokogawa, Yukiko,Sakakibara, Tsutomu

, p. 728 - 729 (2007/10/03)

Novel ruthenium-catalyzed reactions that employ ruthenium trichloride n-hydrate (RuCl3·nH2O) were investigated and dimerization, alkoxylation and sulfidation of olefins were noted. Adducts of Markovnikov type and anti-Markovnikov type were obtained in a stereospecific manner and in good yield, depending on the type of olefins used as the starting materials. (Graph Presented).

Reactions of Copper(I) Halide Complexes of Trivalent Phosphorus with Vinylic Halides

Axelrad, George,Laosooksathit, Surin,Engel, Robert

, p. 5200 - 5204 (2007/10/02)

The direct formation of the vinylic carbon to phosphorus bond has been accomplished via reaction of vinylic halides with copper(I) halide complexes of trialkyl phosphites.In addition, formation of varying amounts of vinylic chlorides may be observed if the reaction is performed by using vinylic bromides with copper(I) chloride complexes of trialkyl phosphites.This halogen-exchange reaction may be made synthetically useful through the employment of copper(I) chloride complexes of triaryl phosphites or phosphines.

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