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34632-89-8

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34632-89-8 Usage

General Description

1-Chloro-2,4-hexadiene is a chemical compound with the molecular formula C6H9Cl. It is a colorless liquid with a pungent odor, and it is classified as a chlorinated hydrocarbon. 1-Chloro-2,4-hexadiene is primarily used as an intermediate in the production of other chemicals, particularly in the synthesis of polymers, agrochemicals, and pharmaceuticals. It is also used as a solvent and as a reagent in organic synthesis. 1-Chloro-2,4-hexadiene is considered to be hazardous, as it is flammable and may cause irritation to the skin, eyes, and respiratory system upon exposure. Therefore, proper safety precautions should be taken when handling and using 1-Chloro-2,4-hexadiene.

Check Digit Verification of cas no

The CAS Registry Mumber 34632-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,3 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34632-89:
(7*3)+(6*4)+(5*6)+(4*3)+(3*2)+(2*8)+(1*9)=118
118 % 10 = 8
So 34632-89-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H9Cl/c1-2-3-4-5-6-7/h2-5H,6H2,1H3

34632-89-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E,4E)-1-chlorohexa-2,4-diene

1.2 Other means of identification

Product number -
Other names sorbyl chloride

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:34632-89-8 SDS

34632-89-8Relevant articles and documents

Preparation of allylboronates by Pd-catalysed borylative cyclisation of dienynes

Lopez-Duran, Ruth,Martos-Redruejo, Alicia,Bunuel, Elena,Pardo-Rodriguez, Virtudes,Cardenas, Diego J.

supporting information, p. 10691 - 10693 (2013/11/06)

Reaction of a variety of dienynes with bis(pinacolato)diboron catalysed by Pd bis(trifluoroacetate) affords allylic boronates containing five or six membered carbo- or heterocycles, by concomitant formation of one C-C and one C-B bonds. Resulting allylboronates can be employed for a variety of subsequent transformations.

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