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1,1-bis(bromomethyl)cyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21623-88-1

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21623-88-1 Usage

Structure

Cyclohexane derivative with two bromomethyl groups attached to the carbon atoms at the 1 position

Usage

Building block for the synthesis of various organic compounds and materials

Applications

Production of polymers, pharmaceuticals, and agrochemicals

Physical state

Colorless, liquid substance

Odor

Strong and pungent

Flammability

Flammable

Health hazard

May cause respiratory irritation if inhaled

Safety precautions

Should be handled and stored carefully, proper safety measures should be taken when working with it

Check Digit Verification of cas no

The CAS Registry Mumber 21623-88-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,2 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21623-88:
(7*2)+(6*1)+(5*6)+(4*2)+(3*3)+(2*8)+(1*8)=91
91 % 10 = 1
So 21623-88-1 is a valid CAS Registry Number.

21623-88-1SDS

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 1,1-bis(bromomethyl)cyclohexane

1.2 Other means of identification

Product number -
Other names 1.1-Bis-<brommethyl>-cyclohexan

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:21623-88-1 SDS

21623-88-1Relevant academic research and scientific papers

Laser-Powered Decomposition of Spiroalkanes (n = 2-5)

Fajgar, Radek,Pola, Josef

, p. 7709 - 7717 (2007/10/02)

The laser heating of spiroalkanes (n=2-5) and of their 1,1,2,2-tetradeuterated isotopomers reveals dissimilar modes of their thermal decomposition.Spiropentane decomposes into ethene and propadiene via two competing routes: the direct cleavage and the more important cleavage via intermediary methylenecyclobutane.Spirohexane decomposes through two important concurrent pathways which are the expulsions of ethene from the three-membered ring and a more feasible expulsion of ethene from the four-membered ring.Spiroheptane and spirooctane decompose by a radical-chain mechanism and afford complex mixtures of products; upon addition of propene both compounds rearrange into two cycloalkanes wherein the larger ring of the spiroalkane is preserved and substituted with ethylidene and a vinyl group.

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