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1202-60-4 Usage

General Description

"(2Z)-3-(4-chlorophenyl)-2-methylprop-2-enoic acid" is a chemical compound with a molecular formula of C10H9ClO2. It is also known as 2Z-4-chlorocinnamic acid and is commonly used in the synthesis of pharmaceuticals, agrochemicals, and organic materials. The compound has a trans geometric isomerism and contains a 4-chlorophenyl group and a methylprop-2-enoic acid moiety. It is a white to off-white crystalline powder that is sparingly soluble in water but soluble in organic solvents. The compound also exhibits anti-inflammatory and antioxidant properties, making it a potential candidate for drug development and research in the medical and pharmaceutical fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1202-60-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1202-60:
34 % 10 = 4
So 1202-60-4 is a valid CAS Registry Number.



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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017


1.1 GHS Product identifier

Product name (Z)-3-(4-chlorophenyl)-2-methylprop-2-enoic acid

1.2 Other means of identification

Product number -
Other names -

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:1202-60-4 SDS

1202-60-4Relevant articles and documents



, p. 4043 - 4047 (1966)


Copper-Photocatalyzed Contra-Thermodynamic Isomerization of Polarized Alkenes

Bouillon, Jean-Philippe,Brégent, Thibaud,Poisson, Thomas

, p. 7688 - 7693 (2020/10/09)

The contra-thermodynamic isomerization of α- and β-substituted cinnamate derivatives catalyzed by the Cu(OAc)2/rac-BINAP complex under blue light irradiation is reported. The use of an oxazolidinone template, which favored the complexation of the copper catalyst to the substrate, allowed the E → Z isomerization of the catalytically formed chromophore under simple and robust reaction conditions in good to excellent ratios. The mechanism of this process based on the transient formation of a chromophore was also studied.

Microwave-assisted synthesis of the (E)-α-methylalkenoate framework from multifunctionalized allylic phosphonium salts

Meier, Lidiane,Ferreira, Misael,Sa, Marcus M.

, p. 179 - 186 (2012/07/14)

A convenient and general microwave-assisted method for the synthesis of stereochemically defined α-methylalkenoic acids and esters from allylic phosphonium salts in a basic aqueous medium is described. A selective preparation of acids or esters was dependent on the base (NaOH or NaHCO 3) employed in the reaction and could be achieved with good to excellent yields under mild conditions in the absence of hydrides and reducing agents.

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