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64473-34-3

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64473-34-3 Usage

General Description

3-(4'-chlorophenyl)propyl chloride is a chemical compound with the molecular formula C9H10Cl2. It is a colorless liquid that is commonly used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. The compound is also a key building block in the production of dyes and pigments. 3-(4'-chlorophenyl)propyl chloride is classified as a chlorinated alkyl chloride, which makes it a useful reagent for the introduction of the 4'-chlorophenylpropyl group in organic synthesis. It is important to handle 3-(4'-chlorophenyl)propyl chloride with care, as it is a corrosive substance that can cause skin and eye irritation upon contact.

Check Digit Verification of cas no

The CAS Registry Mumber 64473-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,4,7 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64473-34:
(7*6)+(6*4)+(5*4)+(4*7)+(3*3)+(2*3)+(1*4)=133
133 % 10 = 3
So 64473-34-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H10Cl2/c10-7-1-2-8-3-5-9(11)6-4-8/h3-6H,1-2,7H2

64473-34-3SDS

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 3-(4'-Chlorophenyl)propyl chloride

1.2 Other means of identification

Product number -
Other names 1-chloro-4-(3-chloropropyl)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:64473-34-3 SDS

64473-34-3Relevant articles and documents

Room temperature C(sp2)-H oxidative chlorination: Via photoredox catalysis

Zhang, Lei,Hu, Xile

, p. 7009 - 7013 (2017/10/05)

Photoredox catalysis has been developed to achieve oxidative C-H chlorination of aromatic compounds using NaCl as the chlorine source and Na2S2O8 as the oxidant. The reactions occur at room temperature and exhibit exclusive selectivity for C(sp2)-H bonds over C(sp3)-H bonds. The method has been used for the chlorination of a diverse set of substrates, including the expedited synthesis of key intermediates to bioactive compounds and a drug.

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