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1,3-Cyclohexadiene,1,2-dichloro-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84565-62-8

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84565-62-8 Usage

Structure

A derivative of cyclohexadiene with two chlorine atoms at the 1,2 positions

Physical state

Colorless liquid

Boiling point

128-130°C

Uses

Intermediate in the production of chemicals such as pharmaceuticals, agrochemicals, and dyes

Reactivity

Chlorinated structure provides unique reactivity in various chemical processes

Safety

Toxic and can cause skin irritation and respiratory damage if inhaled

Handling

Should be handled with care due to its toxic nature and potential for skin and respiratory irritation

Check Digit Verification of cas no

The CAS Registry Mumber 84565-62-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,5,6 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 84565-62:
(7*8)+(6*4)+(5*5)+(4*6)+(3*5)+(2*6)+(1*2)=158
158 % 10 = 8
So 84565-62-8 is a valid CAS Registry Number.

84565-62-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dichlorocyclohexa-1,3-diene

1.2 Other means of identification

Product number -
Other names -

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:84565-62-8 SDS

84565-62-8Downstream Products

84565-62-8Relevant academic research and scientific papers

A SIMPLE ROUTE TO 3-(DIHALOMETHYLENE)CYCLO-ALKENES

Baird, Mark S.,Slowey, Paul D.

, p. 3795 - 3796 (2007/10/02)

Thermolysis of a number of bicyclic trihalocyclopropanes (1;X,Y=halogen) in the presence of quinoline leads either to 3-(dihalomethylene)cyclo-alkenes (8,9,10) with loss of halogen X or to ring expanded 1,2-dihalocycloalka-1,3-dienes (11,13) with loss of halogen Y, depending on ring size and on the nature of the halogen.

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