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Benzenepropanoic acid, a-chloro-4-(phenylmethoxy)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60871-49-0

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60871-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60871-49-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,7 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60871-49:
(7*6)+(6*0)+(5*8)+(4*7)+(3*1)+(2*4)+(1*9)=130
130 % 10 = 0
So 60871-49-0 is a valid CAS Registry Number.

60871-49-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3-(p-benzyloxyphenyl)-2-chloropropanoate

1.2 Other means of identification

Product number -
Other names 3-(4-Benzyloxy-phenyl)-2-chloro-propionic acid methyl ester

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:60871-49-0 SDS

60871-49-0Relevant academic research and scientific papers

Anomalous fluorinations of 3-aryl-2-hydroxypropanoic esters by diethylaminosulfur trifluoride (DAST)

Haigh, David,Jefcott, Lee J.,Magee, Katherine,McNab, Hamish

, p. 2895 - 2900 (2007/10/03)

Treatment of 3-aryl-2-hydroxypropanoic esters 8 with diethylaminosulfur trifluoride (DAST) gives considerable amounts of rearranged 2-aryl-3-fluoropropanoic esters 12 together with the expected products 11. The extent of rearrangement is dependent on solv

Studies on antihyperlipidemic agents. II. Synthesis and biological activities of 2-chloro-3-arylpropionic acids

Kawamatsu,Asakawa,Saraie,Imamiya,Nishikawa,Hamuro

, p. 585 - 589 (2007/10/02)

α-Substituted-β-arylpropionic acid derivatives were prepared and examined for hypolipidemic activity. The structure-activity relationship study showed that a chloro substituent at the α-position and an aryloxy or aralkyloxy substituent on the β-aryl moiet

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