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1-chloro-2,2-dimethylbutane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6366-35-4

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6366-35-4 Usage

Type of compound

Chlorinated hydrocarbon

Physical state

Colorless liquid

Odor

Characteristic odor

Flammability

Flammable

Reactivity

May react with strong oxidizing agents

Uses

a. Solvent in organic synthesis
b. Intermediate in the production of other chemicals
c. Solvent in pharmaceutical and manufacturing industries

Health hazard

Considered hazardous to health

Safety precautions

Should be handled with caution

Check Digit Verification of cas no

The CAS Registry Mumber 6366-35-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,6 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6366-35:
(6*6)+(5*3)+(4*6)+(3*6)+(2*3)+(1*5)=104
104 % 10 = 4
So 6366-35-4 is a valid CAS Registry Number.

6366-35-4SDS

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-chloro-2,2-dimethylbutane

1.2 Other means of identification

Product number -
Other names Butane,1-chloro-2,2-dimethyl

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:6366-35-4 SDS

6366-35-4Relevant academic research and scientific papers

Alkylation of alkyl, cycloalkyl and aralkyl halides

-

, (2008/06/13)

Alkyl, cycloalkyl or aralkyl halides may be alkylated by treatment with an olefin in the presence of a catalyst comprising a free-radical generating compound such as an organic peroxide and also in the presence of a promoter comprising hydrogen chloride, said alkylation reaction being effected at temperatures at least as high as the decomposition temperature of the free-radical generating compound, to prepare alkylated halide-containing compounds.

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