20037-37-0 Usage
Uses
Used in Pharmaceutical Industry:
5-bromo-7-methoxy-1-benzofuran-2-carboxylic acid is used as a building block for the synthesis of bioactive molecules due to its unique chemical structure and potential biological activities, such as anti-inflammatory, antimicrobial, or antioxidant properties. Its versatility allows for the development of new drugs targeting various diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical industry, 5-bromo-7-methoxy-1-benzofuran-2-carboxylic acid is used as an intermediate in the production of pesticides or other agrochemicals. Its chemical properties may contribute to the development of effective and environmentally friendly solutions for pest control and crop protection.
Used in Materials Science:
5-bromo-7-methoxy-1-benzofuran-2-carboxylic acid is utilized in materials science for the development of new materials with specific properties. Its unique structure and functional groups can be exploited to create materials with tailored characteristics for various applications, such as sensors, catalysts, or advanced materials with specific mechanical, electrical, or optical properties.
Used in Scientific Research:
As a valuable target for scientific research, 5-bromo-7-methoxy-1-benzofuran-2-carboxylic acid is used in the study of its biological activities and potential applications. Researchers investigate its interactions with biological systems, mechanisms of action, and possible uses in drug development or other fields, contributing to the advancement of knowledge and the discovery of new applications.
Check Digit Verification of cas no
The CAS Registry Mumber 20037-37-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,3 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20037-37:
(7*2)+(6*0)+(5*0)+(4*3)+(3*7)+(2*3)+(1*7)=60
60 % 10 = 0
So 20037-37-0 is a valid CAS Registry Number.
20037-37-0Relevant academic research and scientific papers
Tandem Synthesis of 2-Carboxybenzofurans via Sequential Cu-Catalyzed C-O Coupling and Mo(CO)6-Mediated Carbonylation Reactions
Mo, Qinliang,Sun, Nan,Jin, Liqun,Hu, Baoxiang,Shen, Zhenlu,Hu, Xinquan
, p. 11490 - 11500 (2020/10/12)
A modular tandem synthesis of 2-carboxybenzofurans from 2-gem-dibromovinylphenols has been established based on a sequence of Cu-catalyzed intramolecular C-O coupling and Mo(CO)6-mediated intermolecular carbonylation reactions. This protocol allowed one-step access to a broad variety of functionalized benzofuran-2-carboxylic acids, esters, and amides in good to excellent yields under Pd- and CO gas-free conditions.
SUBSTITUTED 4-ALKOXYOXAZOL DERIVATIVES AS PPAR AGONISTS
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Page/Page column 27, (2010/02/07)
The present invention relates to compounds of formula (I) wherein R1 to R8 and n are as defined in the description and claims, and pharmaceutically acceptable salts and esters thereof. The compounds are useful for the treatment of diseases such as diabetes.
AROMATIC AMIDINE DERIVATIVES AND SALTS THEREOF
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, (2008/06/13)
An anticoagulant agent which comprises, as an active ingredient, an aromatic amidine derivative represented by the following general formula (1) or a salt thereof: STR1 wherein the group represented by STR2 is a group selected from indolyl, benzofuranyl, benzothienyl, benzimidazolyl, benzoxazolyl, benzothiazolyl, naphthyl, tetrahydronaphthyl and indanyl; X is a single bond, an oxygen atom, a sulfur atom or a carbonyl group; and Y is a saturated or unsaturated 5-or 6-membered heterocyclic moiety or cyclic hydrocarbon moiety optionally having a substituent group, an amino group optionally having a substituent group or an aminoalkyl group optionally having a substituent group.The inventive compound has a high anticoagulant capacity based on its excellent FXa inhibition activity.
