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930-65-4

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930-65-4 Usage

Description

4-Chlorocyclohexene is a 4-substituted cyclohexene, which is an organic compound with a chlorine atom attached to the fourth carbon atom in a cyclohexene ring. It is known for its chemical reactivity and potential applications in various industries.

Uses

Used in Chemical Synthesis:
4-Chlorocyclohexene is used as a chemical intermediate for the synthesis of various organic compounds. Its reactivity allows it to undergo various chemical reactions, making it a valuable building block in the production of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-chlorocyclohexene is used as a key intermediate in the synthesis of various drug molecules. Its unique structure and reactivity enable the development of new drugs with improved therapeutic properties and reduced side effects.
Used in Agrochemical Industry:
4-Chlorocyclohexene is also used in the agrochemical industry for the synthesis of pesticides and other crop protection agents. Its ability to form stable and effective compounds makes it a valuable component in the development of new and improved agrochemical products.
Used in the Synthesis of Bicyclo[3.1.0]hexane Rings:
4-Chlorocyclohexene is used as a starting material for the creation of bicyclo[3.1.0]hexane rings via zirconium y-elimination. This reaction is an important method for the synthesis of complex organic molecules, particularly in the field of organic chemistry and materials science. The resulting bicyclo[3.1.0]hexane rings can be further modified and used in various applications, such as in the development of new pharmaceuticals, agrochemicals, and other specialty chemicals.

Synthesis Reference(s)

Journal of the American Chemical Society, 107, p. 7978, 1985 DOI: 10.1021/ja00312a030

Check Digit Verification of cas no

The CAS Registry Mumber 930-65-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 930-65:
(5*9)+(4*3)+(3*0)+(2*6)+(1*5)=74
74 % 10 = 4
So 930-65-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H9Cl/c7-6-4-2-1-3-5-6/h1-2,6H,3-5H2

930-65-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-CHLOROCYCLOHEXENE

1.2 Other means of identification

Product number -
Other names 4-chloro-cyclohexene

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:930-65-4 SDS

930-65-4Downstream Products

930-65-4Relevant articles and documents

-

Slaugh,L.H.

, p. 1522 - 1526 (1965)

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MECHANISMS OF EPOXIDATIONS AND CHLORINATIONS OF HYDROCARBONS BY INORGANIC HYPOCHLORITE IN THE PRESENCE OF A PHASE-TRANSFER CATALYST.

Fonouni,Krishnan,Kuhn,Hamilton

, p. 7672 - 7676 (2007/10/02)

Inorganic hypochlorite in the presence of a quarternary ammonium salt (phase-transfer catalyst) not only epoxidizes several arenes to arene oxides in high yields but also converts toluene to alpha -chlorotoluene, anisole to ring chlorinated anisoles, and alkenes to a complex mixture of chlorinated and oxidized products, including the epoxide. More detailed studies with this system indicate the following: (1) the high-yield conversion of toluenes to benzyl chlorides proceeds with a deuterium isotope effect of 3. 6 and a rho ** plus value of minus 1. 7: (2) p-chloroanisole is the major product from anisole and is formed in a 22-fold greater quantity than o-chloroanisole; (3) the epoxidation of cis- and trans-alkenes is stereoselective but not completely stereospecific; (4) the chlorination of saturated hydrocarbons occurs with a selectivity that is experimentally identical with that of chlorine monoxide.

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