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"Benzene, 1-(1-butenyl)-4-chloro-, (Z)-" is a chemical compound with the molecular formula C10H13Cl. It is a derivative of benzene, featuring a 1-butenyl group attached to the first carbon atom and a chlorine atom at the fourth carbon position. The "Z" notation indicates the geometric isomerism of the double bond in the 1-butenyl group, with the highest priority substituents being on the same side of the double bond. Benzene, 1-(1-butenyl)-4-chloro-, (Z)- is an aromatic hydrocarbon with a vinyl group, which may be used in organic synthesis or as an intermediate in the production of various chemicals. It is important to handle Benzene, 1-(1-butenyl)-4-chloro-, (Z)- with care due to its potential health and environmental impacts.

7642-14-0

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7642-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7642-14-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,4 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7642-14:
(6*7)+(5*6)+(4*4)+(3*2)+(2*1)+(1*4)=100
100 % 10 = 0
So 7642-14-0 is a valid CAS Registry Number.

7642-14-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-1-(p-chlorophenyl)-1-butene

1.2 Other means of identification

Product number -
Other names 1-((Z)-But-1-enyl)-4-chloro-benzene

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:7642-14-0 SDS

7642-14-0Downstream Products

7642-14-0Relevant academic research and scientific papers

Reactions of polymer-supported α-selenoaldehydes with Grignard regents. A facile solid-phase stereoselective synthesis of (E)-1,2-disubstituted ethenes

Sheng, Shou-Ri,Huang, Xian

, p. 893 - 896 (2007/10/03)

Polymer-supported α-selenoaldehydes easily obtained by reaction of polymer-supported 4-(phenyl-seleno)morpholine with aldehydes react with Grignard reagents to form polymer-supported β-hydroxyalkyl selenides, which were treated with thionyl chloride/triethylamine leading to (E)-1,2-disubstituted ethenes in good yields.

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