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Methyl (2-chloro-4,5-dimethoxyphenyl)acetate is an organic compound with the chemical formula C10H11ClO3. It is a colorless to pale yellow liquid with a molecular weight of 214.65 g/mol. methyl (2-chloro-4,5-dimethoxyphenyl)acetate is characterized by a chlorinated phenyl ring with two methoxy groups attached at the 4 and 5 positions, and a methyl ester group at the 2 position. It is synthesized through the reaction of 2-chloro-4,5-dimethoxyphenol with methyl chloroacetate. Methyl (2-chloro-4,5-dimethoxyphenyl)acetate is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain herbicides and pesticides. Due to its potential applications and chemical properties, it is an important compound in the field of organic chemistry and chemical engineering.

6834-54-4

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6834-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6834-54-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,3 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6834-54:
(6*6)+(5*8)+(4*3)+(3*4)+(2*5)+(1*4)=114
114 % 10 = 4
So 6834-54-4 is a valid CAS Registry Number.

6834-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name <2-Chlor-4,5-dimethoxy-phenyl>-essigsaeure-methylester

1.2 Other means of identification

Product number -
Other names <6-Carboxy-2,4-dinitrophenyl>-pyrimidyl-thioaether

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 -
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More Details:6834-54-4 SDS

6834-54-4Relevant academic research and scientific papers

The synthesis of 2′,2′-bis-benzylisoquinolines and their cytostatic activities

Taylor, Stephen R.,Ung, Alison T.,Pyne, Stephen G.

, p. 10896 - 10901 (2008/03/17)

The novel laudanosine dimers in which two laudanosine units are linked via a C-2′ biaryl bond have been prepared by a sequence that involves formation of the biaryl bond first and then formation of the isoquinoline rings. Two of these compounds showed higher cytostatic activity on three cancer cell lines than thalicarpine. Crown Copyright

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