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21676-01-7

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21676-01-7 Usage

General Description

(Z)-1-chlorohex-3-ene is a chemical compound with the molecular formula C6H11Cl. It is an alkene, meaning it contains a carbon-carbon double bond, and the chlorine atom is attached to the first carbon of the chain. (Z)-1-chlorohex-3-ene is often used in organic synthesis and chemical reactions due to its reactivity and potential for forming new carbon-carbon bonds. It is a flammable liquid with a sharp, unpleasant odor, and should be handled with caution. (Z)-1-chlorohex-3-ene is also important in the production of various industrial and pharmaceutical products, making it a valuable chemical in the field of organic chemistry and chemical manufacturing.

Check Digit Verification of cas no

The CAS Registry Mumber 21676-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,7 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21676-01:
(7*2)+(6*1)+(5*6)+(4*7)+(3*6)+(2*0)+(1*1)=97
97 % 10 = 7
So 21676-01-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H11Cl/c1-2-3-4-5-6-7/h3-4H,2,5-6H2,1H3/b4-3-

21676-01-7SDS

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 (Z)-1-chlorohex-3-ene

1.2 Other means of identification

Product number -
Other names cis-1-Chlor-hex-3-en

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:21676-01-7 SDS

21676-01-7Relevant articles and documents

-

Bergel'son,L.D. et al.

, (1968)

-

Enzyme-triggered enantioconvergent transformation of haloalkyl epoxides

Mayer, Sandra F.,Steinreiber, Andreas,Orru, Romano V. A.,Faber, Kurt

, p. 4537 - 4542 (2007/10/03)

Biocatalytic hydrolysis of 2,3-disubstituted rac-cis- and rac-trans-haloalkyl epoxides 1a-8a using the epoxide hydrolase activity of whole bacterial cells furnished the corresponding vicinal diols 1b-8b as intermediates; these (spontaneously) underwent ring closure to yield cyclic products 1c-6c through an enzyme-triggered cascade reaction. In particular, cis-configured substrates (1a, 3a, 5a, 7a) were transformed in an enantioconvergent fashion, which resulted in the formation of single stereoisomeric products in 100% des and up to 92% ees from the racemates.

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