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2-Benzofurancarboxylic acid, 5,6-dihydroxy-3-methyl-(8CI) is a chemical compound with the molecular formula C10H8O5. It belongs to the class of benzofuran derivatives, which are heterocyclic compounds consisting of a benzene ring fused to a furan ring. This specific compound features a carboxylic acid group (-COOH) attached to the benzofuran structure, along with two hydroxyl groups (-OH) at the 5 and 6 positions, and a methyl group (-CH3) at the 3 position. The compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in organic chemistry. Its unique structure and functional groups make it an interesting target for further research and development in the field of chemistry.

21452-90-4

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21452-90-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21452-90-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,5 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21452-90:
(7*2)+(6*1)+(5*4)+(4*5)+(3*2)+(2*9)+(1*0)=84
84 % 10 = 4
So 21452-90-4 is a valid CAS Registry Number.

21452-90-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-Dihydroxy-3-methyl-1-benzofuran-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-methyl-DHFCA

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:21452-90-4 SDS

21452-90-4Downstream Products

21452-90-4Relevant academic research and scientific papers

GPR35 LIGANDS AND THE USES THEREOF

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Paragraph 0389; 393; 0399, (2013/03/26)

Disclosed are compositions and methods for reducing the risk of and/or treatment of diseases which are pathophysiologically related to GPR35, and/or GPR35-hERG signaling complex. For example, disclosed are compounds for reducing the risk of and/or treatin

Synthesis and agonistic activity at the GPR35 of 5,6-dihydroxyindole-2- carboxylic acid analogues

Deng, Huayun,Fang, Ye

, p. 550 - 554 (2012/09/05)

5,6-Dihydroxyindole-2-carboxylic acid (DHICA), an intermediate of melanin synthesis and an eumelanin building block, was recently discovered to be a GPR35 agonist with moderate potency. Here, we report the synthesis and pharmacological characterization of a series of DHICA analogues against GPR35 using both label-free dynamic mass redistribution and Tango β-arrestin translocation assays. This led to identification of novel GPR35 agonists with improved potency and/or having biased agonism.

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