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1,3-Cyclohexadiene,1,4-dichloro-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71786-18-0

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71786-18-0 Usage

Physical state

Colorless liquid

Molecular weight

147.01 g/mol

Usage

a. Reagent in chemical synthesis processes
b. Formation of other organic compounds
c. Intermediate in the production of pharmaceuticals and agrochemicals

Hazardous properties

Flammable and potentially hazardous

Safety precautions

Proper handling and storage required

Check Digit Verification of cas no

The CAS Registry Mumber 71786-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,7,8 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 71786-18:
(7*7)+(6*1)+(5*7)+(4*8)+(3*6)+(2*1)+(1*8)=150
150 % 10 = 0
So 71786-18-0 is a valid CAS Registry Number.

71786-18-0SDS

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 1,4-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:71786-18-0 SDS

71786-18-0Downstream Products

71786-18-0Relevant academic research and scientific papers

Rearrangements of 1,6-Dihalotricyclo2,5>decanes. Synthesis of Tricyclo4,8>decane Derivatives

Wiseman, John R.,Vanderbilt, Jeffrey J.,Butler, William M.

, p. 667 - 671 (1980)

1,8-Diiodotricyclo4,8>decane (16) was prepared by reaction of 1,6-dihalotricyclo2,5>decanes 9a and 9b with aluminum triiodide.Reduction of 16 with n-butyltin dihydride produced the tricyclic hydrocarbon tricyclo4,8>decane (1).Dichloride 9a was prepared by a Diels-Alder reaction between 1,4-dichlorocyclohexa-1,3-diene (10a) and cyclobutene followed by catalytic hydrogenation of the adduct 12a.The structure of 16 was determined by an X-ray diffraction study of a single crystal.

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