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methyl 2,3,4,5-tetrachlorobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90348-16-6

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90348-16-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90348-16-6 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, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90348-16:
(7*9)+(6*0)+(5*3)+(4*4)+(3*8)+(2*1)+(1*6)=126
126 % 10 = 6
So 90348-16-6 is a valid CAS Registry Number.

90348-16-6SDS

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 methyl 2,3,4,5-tetrachlorobenzoate

1.2 Other means of identification

Product number -
Other names 2,3,4,5-tetrachloro-benzoic 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:90348-16-6 SDS

90348-16-6Downstream Products

90348-16-6Relevant academic research and scientific papers

Rhodium-Catalyzed Double Alkyl-Oxygen Bond Cleavage: An Alkyl Transfer Reaction from Bis/Tris(o-alkyloxyphenyl)phosphine to Aryl Acids

Zhou, Hui,Zhang, Jinlong,Yang, Huameng,Xia, Chungu,Jiang, Gaoxi

supporting information, p. 3406 - 3412 (2016/10/21)

An unprecedented rhodium-catalyzed selective cleavage of double alkyl-oxygen bonds of bis/tris(o-alkyloxyphenyl)phosphine has been realized, in which P atom functions as a directing group and simple aryl acids are the methyl group acceptor to provide methyl esters and a quaternary phosphonium salt. The preliminary mechanism was investigated via an 18O labeling experiment and stoichiometric reaction between a Rh-A crystal and an aromatic acid.

Participation of Solvent Dimethylformamide during Attempted Nucleophilic Displacement of Chlorine in Tetrachlorophthalic Anhydride

Ramadas, Sukuru R.,Pillai, Chandrasekaran N.,Bakthavatchalam, Rajagopal

, p. 1059 - 1060 (2007/10/02)

The interaction of tetrachlorophthalic anhydride with dimethylformamide at its reflux temperature either in the presence or absence of an aryl oxide or alkoxide furnishes predominently N,N-dimethyl-2,3,4,5-tetrachlorobenzamide (3) in contrast to the corresponding acid (4), as reported in literature.

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