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4730-24-9

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4730-24-9 Usage

General Description

2-Bromo-6-methylheptane, also known as 2-bromo-6-methylheptane, is a chemical compound with the molecular formula C8H17Br. It is a branched chain alkane with a bromine atom attached to the second carbon of the heptane chain and a methyl group attached to the sixth carbon. This chemical is commonly used as a reagent in organic synthesis, particularly for the preparation of other organic compounds. It is a colorless liquid with a strong odor and is flammable. 2-Bromo-6-methylheptane is used in various industries including pharmaceuticals, agrochemicals, and chemical intermediates. It is important to handle this compound with care due to its flammability and potential health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 4730-24-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,3 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4730-24:
(6*4)+(5*7)+(4*3)+(3*0)+(2*2)+(1*4)=79
79 % 10 = 9
So 4730-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H17Br/c1-7(2)5-4-6-8(3)9/h7-8H,4-6H2,1-3H3

4730-24-9SDS

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 2-BROMO-6-METHYLHEPTANE

1.2 Other means of identification

Product number -
Other names 2-bromo-6-methyl-heptane

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:4730-24-9 SDS

4730-24-9Relevant articles and documents

The synthesis of trisubstituted cyclopentadienes and their reactivity in the intramolecular Diels-Alder reaction

Alward, Sandra J.,Fallis, Alex G.

, p. 121 - 127 (2007/10/02)

The intramolecular Diels-Alder reactivity of several trisubstituted cyclopentadienes is described and a general method for their preparation reported.In general, sidechain keto-ester functionality has an adverse effect on these internal cycloadditions.

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