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4032-86-4

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4032-86-4 Usage

General Description

3,3-Dimethylheptane is a chemical compound classified as an alkane, which is part of the hydrocarbon family. Its molecular formula is C9H20, indicating it has nine carbon and twenty hydrogen atoms. 3,3-Dimethylheptane is a saturated organic compound that is highly volatile and flammable. It is found in crude oils and produced as a by-product during the refining process. It is usually used in research and for various industrial applications. The presence of two methyl groups in its structure makes it more prone to reactions compared to normal heptane. It has a boiling point of 166–167 °C.

Check Digit Verification of cas no

The CAS Registry Mumber 4032-86-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,3 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4032-86:
(6*4)+(5*0)+(4*3)+(3*2)+(2*8)+(1*6)=64
64 % 10 = 4
So 4032-86-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H20/c1-5-7-8-9(3,4)6-2/h5-8H2,1-4H3

4032-86-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-Dimethylheptane

1.2 Other means of identification

Product number -
Other names 3,3-DIMETHYLHEPTANE

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:4032-86-4 SDS

4032-86-4Relevant 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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