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2-Propenoic acid, 3-(3,4-dimethoxyphenyl)-2-hydroxy-, methyl ester is a complex organic compound with the chemical formula C12H14O5. It is a derivative of 2-propenoic acid, featuring a 3,4-dimethoxyphenyl group attached to the 3-position of the propenoic acid backbone. The molecule also contains a hydroxyl group at the 2-position and a methyl ester group, which is a methyl group (CH3) attached to the carboxylic acid group, forming an ester. 2-Propenoic acid, 3-(3,4-dimethoxyphenyl)-2-hydroxy-, methyl ester is known for its potential applications in the pharmaceutical and chemical industries, particularly as an intermediate in the synthesis of various drugs and other organic compounds. Its structure and properties make it a versatile building block for the creation of more complex molecules.

188896-01-7

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188896-01-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 188896-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,8,9 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 188896-01:
(8*1)+(7*8)+(6*8)+(5*8)+(4*9)+(3*6)+(2*0)+(1*1)=207
207 % 10 = 7
So 188896-01-7 is a valid CAS Registry Number.

188896-01-7SDS

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 methyl 3-(3,4-dimethoxyphenyl)-2-hydroxyprop-2-enoate

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

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More Details:188896-01-7 SDS

188896-01-7Relevant academic research and scientific papers

Chemocontrolled reduction of aromatic α-ketoesters by NaBH4: Selective synthesis of α-hydroxy esters or 1,2-diols

Dalla, Vincent,Cotelle, Philippe,Catteau, Jean Pierre

, p. 1577 - 1580 (2007/10/03)

α-Hydroxyesters 5a-g or diols 6a-g have been obtained in high yields by reduction of aromatic α-ketoesters 4 once or twice respectively by using NaBH4 as the reducer under suitable conditions. The use of a solvent that does not interact with the reagent allowed the double reduction to occur with only a slight excess of borohydride in very mild conditions.

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