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2064-03-1

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2064-03-1 Usage

Compound type

Chlorinated derivative of norbornane (a bicyclic organic compound)

Physical state at room temperature

Colorless liquid

Usage

Synthesis of various organic compounds, building block in pharmaceutical and chemical industries, solvent, and in the manufacture of plastics and adhesives

Industrial significance

Unique molecular structure and properties important in various industrial applications

Check Digit Verification of cas no

The CAS Registry Mumber 2064-03-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,6 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2064-03:
(6*2)+(5*0)+(4*6)+(3*4)+(2*0)+(1*3)=51
51 % 10 = 1
So 2064-03-1 is a valid CAS Registry Number.

2064-03-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chlorobicyclo[2.2.2]octane

1.2 Other means of identification

Product number -
Other names 1-Chlor-bicyclo[2.2.2]octan

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:2064-03-1 SDS

2064-03-1Upstream product

2064-03-1Downstream Products

2064-03-1Relevant articles and documents

PREPARATION OF SOME ALKYL CHLORIDES BY DECOMPOSITION OF ALKOXYPHOSPHONIUM CHLORIDES AND BICHLORIDES

Denney, Donald B.,Garth, Bruce H.,Hanifin, J. William Jr.,Relles, Howars M.

, p. 275 - 280 (2007/10/02)

A number of alkoxyphosphonium chlorides and bichlorides have been prepared as stable intermediates or transient species.The thermal decompositions of these salts have been studied under a variety of conditions.The salts decompose by SN2 and SN1 processes in a fairly predictable manner.There are two decided advantages to using these salts as precursors to alkyl halides.The first is that in systems that are normally prone to rearrangements under substitution conditions, the products of decompositions of the salts are often formed with less rearrangement than is often found in other systems.The second is that the phosphates and phosphine oxides are excellent leaving groups and thus substitutions can be effected at centers that normally react very slowly.

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