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methyl 2-(2-hydroxy-4-methoxyphenyl)-2-oxoethanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

299957-46-3

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299957-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 299957-46-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,9,9,5 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 299957-46:
(8*2)+(7*9)+(6*9)+(5*9)+(4*5)+(3*7)+(2*4)+(1*6)=233
233 % 10 = 3
So 299957-46-3 is a valid CAS Registry Number.

299957-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(2-hydroxy-4-methoxyphenyl)-2-oxoethanoate

1.2 Other means of identification

Product number -
Other names (2-hydroxy-4-methoxy-phenyl)-glyoxylic 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:299957-46-3 SDS

299957-46-3Relevant academic research and scientific papers

TAK1 KINASE INHIBITORS, COMPOSITIONS, AND USED RELATED THERETO

-

Page/Page column 51, (2013/03/26)

The disclosure relates to TAK1 inhibitors, compositions, and uses related thereto. In certain embodiments, the disclosure relates to compounds of formula (I), pharmaceutical compositions having a compound of formula (I), and methods of treating or prevent

Hydrogen-atom abstraction/cyclization in synthesis. Direct syntheses of coumestan and coumestrol

Kraus, George A.,Zhang, Ning

, p. 5644 - 5646 (2007/10/03)

The synthesis of coumestrol has been achieved in five steps from 1,3-dimethoxybenzene. The key step is a photochemical cyclization of a glyoxylate ester.

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