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

353504-67-3

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353504-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 353504-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,3,5,0 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 353504-67:
(8*3)+(7*5)+(6*3)+(5*5)+(4*0)+(3*4)+(2*6)+(1*7)=133
133 % 10 = 3
So 353504-67-3 is a valid CAS Registry Number.

353504-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-(2-aminobenzoyl)furan-2-carboxylate

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:353504-67-3 SDS

353504-67-3Relevant academic research and scientific papers

COMPOUNDS, COMPOSITIONS AND METHODS

-

, (2008/06/13)

The present invention provides methods and pharmaceutical compositions for inhibiting expressions of HIF and HIF regulated genes, inhibiting angiogenesis, inducing cell cycle arrest in tumor cells, and treating cell proliferating diseases or conditions.

A Convenient Route to the Soluble Guanylate Cyclase Activator YC-1 and its N2 Regioisomer

Fernandez, Patricia A.,Bellamy, Tom,Kling, Marcel,Madge, David J.,Selwood, David L.

, p. 1813 - 1816 (2007/10/03)

A new route to the soluble guanylate cyclase (sGC) activator YC-1 and its N2 regioisomer has been established with a Mitsunobu mediated N-alkylation as the key step. The route is utilised in the synthesis of a potential photoaffinity label.

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