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10524-08-0

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10524-08-0 Usage

Classification

Alkene (due to carbon-carbon double bond)

Physical state

Clear, colorless liquid

Molecular weight

100.58 g/mol

Uses

Chemical intermediate for production of other organic compounds (pharmaceuticals, agrochemicals, polymers), flavors, fragrances

Reactivity

Moderate, undergoes addition reactions with nucleophiles and electrophiles

Safety precautions

Potential toxicity and flammability, handle with care.

Check Digit Verification of cas no

The CAS Registry Mumber 10524-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,2 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10524-08:
(7*1)+(6*0)+(5*5)+(4*2)+(3*4)+(2*0)+(1*8)=60
60 % 10 = 0
So 10524-08-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H9Cl/c1-3-4-5(2)6/h3,5H,1,4H2,2H3

10524-08-0SDS

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 4-chloropent-1-ene

1.2 Other means of identification

Product number -
Other names 1-Pentene, 4-chloro-

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:10524-08-0 SDS

10524-08-0Relevant articles and documents

CaF2 catalyzed SN2 type chlorodehydroxylation of chiral secondary alcohols with thionyl chloride: A practical and convenient approach for the preparation of optically active chloroalkanes

Zhang, Junjie,Wang, Huanxia,Ma, Yun,Wang, Youming,Zhou, Zhenghong,Tang, Chuchi

, p. 2261 - 2263 (2013/05/09)

A CaF2 catalyzed chlorodehydroxylation of chiral secondary alcohols with thionyl chloride has been developed. The chlorination reaction is effective for a wide range of alcohols, generating the corresponding chloroalkanes in good yield with high optical purity with inversion of the original configuration of the alcohol.

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