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90348-64-4

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90348-64-4 Usage

General Description

(4-chlorophenyl) 3-chloropropanoate is a chemical compound with the molecular formula C9H8Cl2O2. It is a ester of 4-chlorophenyl and 3-chloropropanoic acid. (4-chlorophenyl) 3-chloropropanoate is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used as a solvent in the manufacturing of various products. (4-chlorophenyl) 3-chloropropanoate is known for its potential to cause skin and eye irritation and thus should be handled with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 90348-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,4 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 90348-64:
(7*9)+(6*0)+(5*3)+(4*4)+(3*8)+(2*6)+(1*4)=134
134 % 10 = 4
So 90348-64-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H8Cl2O2/c10-6-5-9(12)13-8-3-1-7(11)2-4-8/h1-4H,5-6H2

90348-64-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-chlorophenyl) 3-chloropropanoate

1.2 Other means of identification

Product number -
Other names 4'-chlorophenyl-3-chloropropionate

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:90348-64-4 SDS

90348-64-4Relevant articles and documents

Preparation process of 7-chlorine-4-hydroxyl dihydroindene

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Paragraph 0020; 0021, (2018/09/11)

The invention discloses a preparation process of 7-chlorine-4-hydroxyl dihydroindene in the field of the organic chemical industry. The preparation process comprises the following steps: (1) carryingout phenol hydroxyl esterification reaction via p-chloro

Bicyclic amino-substituted compounds

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, (2008/06/13)

A compound of formula (I), wherein X is O, CH 2, S, SO or SO 2 ; R is F or Cl; R 1 is H, C 1 -C 6 alkyl or C 2 -C 6 alkenyl; R 2 is H, C 1 -C 6 alkyl or C 2 -C 6 alkenyl; R 3 is H, C 1 -C 6, alkyl, a pharmaceutically acceptable salt thereof, an enantiomer thereof, and a pharmaceutically acceptable salt of said enantiomer for use in therapy. A pharmaceutical preparation containing as active ingredient any one of said compounds. A process for the preparation of a compound of formula (I).

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