64389-22-6

Basic information

• Product Name: 3-(5-BROMO-THIOPHEN-2-YL)-ACRYLIC ACID METHYL ESTER
• Synonyms: 2-Propenoic acid, 3-(5-bromo-2-thienyl)-, methyl ester
• CAS NO: 64389-22-6
• Molecular Formula: C8H7BrO2S
• Molecular Weight: 247.11
• Mol File: 64389-22-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 312.1°C at 760 mmHg
• Flash Point: 142.6°C
• Appearance: /
• Density: 1.583g/cm³
• Vapor Pressure: 0.000539mmHg at 25°C
• Refractive Index: 1.617
• CAS DataBase Reference: 3-(5-BROMO-THIOPHEN-2-YL)-ACRYLIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(5-BROMO-THIOPHEN-2-YL)-ACRYLIC ACID METHYL ESTER(64389-22-6)
• EPA Substance Registry System: 3-(5-BROMO-THIOPHEN-2-YL)-ACRYLIC ACID METHYL ESTER(64389-22-6)

Safety Data

• Hazardous Substances Data: 64389-22-6(Hazardous Substances Data)

Usage

General Description

3-(5-Bromo-thiophen-2-yl)-acrylic acid methyl ester is a chemical compound with the molecular formula C8H7BrO2S. It is an organobromine compound that contains a thiophene ring and an acrylic acid moiety. This chemical is commonly used as a building block in organic synthesis and drug discovery. It is also used as a reagent in chemical reactions to introduce the 3-(5-bromo-thiophen-2-yl)-acrylic acid methyl ester group into organic molecules. Additionally, it has potential applications in the development of new materials and as a starting material in the production of pharmaceuticals. Overall, this compound has diverse applications in the fields of chemistry and material science.

InChI:InChI=1/C8H7BrO2S/c1-11-8(10)5-3-6-2-4-7(9)12-6/h2-5H,1H3/b5-3+

Upstream product

• 4701-17-1 5-bromo-2-thiophencarboxaldehyde 
• 21204-67-1 methyl (triphenylphosphoranylidene)acetate 
• 67-56-1 methanol 
• 50868-68-3 (E)-3-(5-bromo-2-thienyl)-2-propenoic acid 

Relevant articles and documents

Chemical switching in reaction behavior of azine: Synthesis of a novel thienodiazepine derivative

We previously have reported that an acid-promoted condensation of a hydrazonoester derived from phenylalanine afforded an azine which was converted to a pyrrole through 3 steps: isomerization to dienamine, [3,3]-sigmatropic rearrangement, and cyclization.

NOVEL COMPOUNDS THAT MODULATE PPARγ TYPE RECEPTORS, AND USE THEREOF IN COSMETIC OR PHARMACEUTICAL COMPOSITIONS

The invention relates to novel compounds corresponding to the general formula (I) below: and also to the method for preparing them, and to their use in pharmaceutical compositions intended for use in human or veterinary medicine (in dermatology, and also

Water is an efficient medium for Wittig reactions employing stabilized ylides and aldehydes

Water is demonstrated to be an excellent medium for the Wittig reaction employing stabilized ylides and aldehydes. Although the solubility in water appears to be an unimportant characteristic in achieving good chemical yields and E/Z-ratios, the rate of W