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7146-60-3

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7146-60-3 Usage

General Description

2,3-DIMETHYL OCTANE is a chemical compound that belongs to the class of alkanes, also known as saturated hydrocarbons. It is a colorless liquid with a faint odor, and is primarily used as a solvent in various industrial processes. Its chemical formula is C10H22, and it has a molecular weight of 142.28 g/mol. 2,3-DIMETHYL OCTANE is flammable and should be stored and handled with care. It is also used as a reference compound in gas chromatography and is a component in the production of fuels and lubricants.

Check Digit Verification of cas no

The CAS Registry Mumber 7146-60-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7146-60:
(6*7)+(5*1)+(4*4)+(3*6)+(2*6)+(1*0)=93
93 % 10 = 3
So 7146-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H22/c1-5-6-7-8-10(4)9(2)3/h9-10H,5-8H2,1-4H3

7146-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dimethyloctane

1.2 Other means of identification

Product number -
Other names 2,3-dimethyl-octane

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:7146-60-3 SDS

7146-60-3Downstream Products

7146-60-3Relevant articles and documents

IONIC ALKYLATION OF TERTIARY ALKYL HALIDES WITH TETRAALKYLSILANES

Bolestova, G. I.,Parnes, Z. N.

, p. 32 - 36 (2007/10/02)

In the reaction of tertiary alkyl halides with tetraethyl-, tetrapropyl-, tetrabutyl-, and tetraamylsilane in the presence of AlX3 the halogen atom is substituted by the alkyl group with the formation of the corresponding saturated hydrocarbons containing a quaternary carbon atom.As a result of the hydride mobility of the β-hydrogen atom in the tetraalkylsilane ionic hydrogenolysis of the substrate occurs in addition to alkylation, and the degree of hydrogenolysis depends on the alkyl substituent in the silane.

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