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2-Thiophenecarboxylic acid, 5-bromo-4-fluoro-, methyl ester is an organic compound with the chemical formula C8H6BrFO2S. It is a methyl ester derivative of 2-thiophenecarboxylic acid, characterized by its 5-bromo-4-fluoro substitution. 2-Thiophenecarboxylic acid, 5-bromo-4-fluoro-, methyl ester is known for its unique structure and properties, making it a valuable component in organic synthesis and pharmaceutical research.

395664-59-2

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395664-59-2 Usage

Uses

Used in Organic Synthesis:
2-Thiophenecarboxylic acid, 5-bromo-4-fluoro-, methyl ester is used as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure allows for versatile chemical reactions, enabling the synthesis of a wide range of compounds with diverse applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-Thiophenecarboxylic acid, 5-bromo-4-fluoro-, methyl ester is used as a building block for the development of new drugs. Its unique chemical properties make it a promising candidate for the synthesis of novel therapeutic agents with potential applications in various medical fields.
Used in Chemical Research:
2-Thiophenecarboxylic acid, 5-bromo-4-fluoro-, methyl ester is also utilized in chemical research to study the reactivity and properties of substituted thiophenes. Understanding the behavior of 2-Thiophenecarboxylic acid, 5-bromo-4-fluoro-, methyl ester can provide valuable insights into the development of new synthetic methods and the design of novel chemical compounds.
Safety Precautions:
It is important to handle 2-Thiophenecarboxylic acid, 5-bromo-4-fluoro-, methyl ester with caution, as it can be hazardous if not used properly. Proper safety measures, such as wearing protective gear and working in a well-ventilated area, should be taken to minimize the risk of exposure and potential health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 395664-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,5,6,6 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 395664-59:
(8*3)+(7*9)+(6*5)+(5*6)+(4*6)+(3*4)+(2*5)+(1*9)=202
202 % 10 = 2
So 395664-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H4BrFO2S/c1-10-6(9)4-2-3(8)5(7)11-4/h2H,1H3

395664-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-bromo-4-fluorothiophene-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Thiophenecarboxylic acid,5-bromo-4-fluoro-,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:395664-59-2 SDS

395664-59-2Relevant academic research and scientific papers

3-OXO-TETRAHYDRO-FURO[3,2-B]PYRROL-4(5H)-YL) DERIVATIVES I

-

, (2015/11/16)

The invention relates to amidic oxotetrahydro-2H-furo[3.2-b]pyrrol-4(5H)-yl) derivatives as dual CatS/K inhibitors, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.

Ring fluorinated thiophenes: Applications to liquid crystal synthesis

Kiryanov, Andre A.,Seed, Alexander J.,Sampson, Paul

, p. 8797 - 8800 (2007/10/03)

Ring fluorinated thiophenes were synthesized via a Balz-Schiemann fluorination approach and were successfully employed in the synthesis of liquid crystals using regioselective electrophilic bromination and regioselective Suzuki coupling chemistry.

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