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Benzenepropanoic acid, 5-chloro-2-(methoxycarbonyl)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

252989-39-2

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252989-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 252989-39-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,9,8 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 252989-39:
(8*2)+(7*5)+(6*2)+(5*9)+(4*8)+(3*9)+(2*3)+(1*9)=182
182 % 10 = 2
So 252989-39-2 is a valid CAS Registry Number.

252989-39-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-chloro-2-(3-methoxy-3-oxopropyl)benzoate

1.2 Other means of identification

Product number -
Other names methyl 5-chloro-2-(methoxycarbonyl)benzenepropanoate

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:252989-39-2 SDS

252989-39-2Relevant academic research and scientific papers

Substituted cinnamic acids and cinnamic acid esters

-

, (2008/06/13)

The invention relates to substituted cinnamic acids and cinnamic acid esters of formula (I), wherein X represents F, Cl or J and R1and R2are the same or different and represent hydrogen, an optionally substituted C1-C

Preparation of arthropodicidal oxadiazines

-

, (2008/06/13)

A method for making arthropodicidal oxadiazines and intermediates which are racemic or enantiomerically enriched at their chiral center, the method for making the oxadiazines comprising reaction of an intermediate selected from STR1 wherein: R1 is F, Cl, or C1 -C3 fluroalkoxy, R2 is C1 -C3 alkyl, and R4 is H or CO2 CH2 (C6 H5). as well as certain selected intermediates including those depicted above, and methods of making them.

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