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Methyl 3-bromobenzofuran-5-carboxylate is a chemical compound with the formula C10H7BrO3. It is a methyl ester derivative of 3-bromobenzofuran-5-carboxylic acid, which is a heterocyclic aromatic compound. This chemical is commonly used as a building block in organic synthesis and medicinal chemistry.

501892-90-6

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501892-90-6 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 3-bromobenzofuran-5-carboxylate is used as a building block for the development of pharmaceuticals, due to its potential applications in creating various biologically active compounds.
Used in Agrochemical Industry:
Methyl 3-bromobenzofuran-5-carboxylate is used as a precursor in the synthesis of agrochemicals, contributing to the development of effective and targeted pest control solutions.
Used in Fine Chemicals Industry:
Methyl 3-bromobenzofuran-5-carboxylate is utilized in the production of other fine chemicals, showcasing its diverse reactivity and versatility in chemical synthesis.
It is important to handle and use Methyl 3-bromobenzofuran-5-carboxylate with proper safety precautions due to its potential hazards and risks associated with handling organic bromine compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 501892-90-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,8,9 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 501892-90:
(8*5)+(7*0)+(6*1)+(5*8)+(4*9)+(3*2)+(2*9)+(1*0)=146
146 % 10 = 6
So 501892-90-6 is a valid CAS Registry Number.

501892-90-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3-bromo-1-benzofuran-5-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 3-bromobenzofuran-5-carboxylate

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:501892-90-6 SDS

501892-90-6Relevant academic research and scientific papers

Design, synthesis and structure-activity relationships of 1,3,4-oxadiazole derivatives as novel inhibitors of glycogen synthase kinase-3β

Saitoh, Morihisa,Kunitomo, Jun,Kimura, Eiji,Hayase, Yoji,Kobayashi, Hiromi,Uchiyama, Noriko,Kawamoto, Tomohiro,Tanaka, Toshimasa,Mol, Clifford D.,Dougan, Douglas R.,Textor, Garret S.,Snell, Gyorgy P.,Itoh, Fumio

experimental part, p. 2017 - 2029 (2009/05/26)

Glycogen synthase kinase-3β (GSK-3β) is implicated in abnormal hyperphosphorylation of tau protein and its inhibitors are expected to be a promising therapeutic agents for the treatment of Alzheimer's disease. Here we report design, synthesis and structure-activity relationships of a novel series of oxadiazole derivatives as GSK-3β inhibitors. Among these inhibitors, compound 20x showed highly selective and potent GSK-3β inhibitory activity in vitro and its binding mode was determined by obtaining the X-ray co-crystal structure of 20x and GSK-3β.

2-{3-[4-(Alkylsulfinyl)phenyl]-1-benzofuran-5-yl}-5-methyl-1,3,4-oxadiazole derivatives as novel inhibitors of glycogen synthase kinase-3β with good brain permeability

Saitoh, Morihisa,Kunitomo, Jun,Kimura, Eiji,Iwashita, Hiroki,Uno, Yumiko,Onishi, Tomohiro,Uchiyama, Noriko,Kawamoto, Tomohiro,Tanaka, Toshimasa,Mol, Clifford D.,Dougan, Douglas R.,Textor, Garret P.,Snell, Gyorgy P.,Takizawa, Masayuki,Itoh, Fumio,Kori, Masakuni

experimental part, p. 6270 - 6286 (2010/03/24)

Glycogen synthase kinase 3β (GSK-3β) inhibition is expected to be a promising therapeutic approach for treating Alzheimer's disease. Previously we reported a series of 1,3,4-oxadiazole derivatives as potent and highly selective GSK-3β inhibitors, however,

Azabicyclic compounds for the treatment of disease

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Page 46, (2010/02/06)

The invention provides compounds of Formula I: 1wherein Azabicyclo is 2These compounds may be in the form of pharmaceutical salts or compositions, may be in pure enantiomeric form or racemic mixtures, and are useful in pharmaceuticals in which α7 is known to be involved.

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