29421-75-8

Basic information

• Product Name: 4-Bromo-5-methyl-2-thiophenecarbaldehyde
• Synonyms: 4-Bromo-5-methylthiophene-2-carboxadehyde;4-Bromo-5-methylthiophene-2-carbaldehyde
• CAS NO: 29421-75-8
• Molecular Formula: C₆H₅BrOS
• Molecular Weight: 205.0723
• Mol File: 29421-75-8.mol
• Article Data: 28

Chemical Properties

• Boiling Point: 266.767 °C at 760 mmHg
• Flash Point: 115.137 °C
• Appearance: /
• Density: 1.667 g/cm³
• CAS DataBase Reference: 4-Bromo-5-methyl-2-thiophenecarbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Bromo-5-methyl-2-thiophenecarbaldehyde(29421-75-8)
• EPA Substance Registry System: 4-Bromo-5-methyl-2-thiophenecarbaldehyde(29421-75-8)

Safety Data

• Hazardous Substances Data: 29421-75-8(Hazardous Substances Data)

Usage

Description

4-Bromo-5-methyl-2-thiophenecarbaldehyde is a chemical compound characterized by the molecular formula C7H7BrOS. It presents as a yellow to brown liquid with a distinctive strong, pungent odor. 4-Bromo-5-methyl-2-thiophenecarbaldehyde is recognized for its utility as an intermediate in the synthesis of various products, including pharmaceuticals and agrochemicals, as well as in the creation of dyes and pigments. Its role as a versatile building block in organic chemistry is highlighted by its ability to serve as a precursor to a multitude of derivatives with diverse functional groups and applications. 4-Bromo-5-methyl-2-thiophenecarbaldehyde also holds promise in medicinal chemistry, with potential biological activity as an antimicrobial or antifungal agent.

Uses

Used in Pharmaceutical and Agrochemical Industries:
4-Bromo-5-methyl-2-thiophenecarbaldehyde is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals for its ability to contribute to the development of new drugs and pesticides, enhancing their efficacy and properties.
Used in Dye and Pigment Production:
In the dye and pigment industry, 4-Bromo-5-methyl-2-thiophenecarbaldehyde is utilized as a key component in the production of various dyes and pigments, contributing to their color and stability.
Used as a Building Block in Organic Chemistry:
4-Bromo-5-methyl-2-thiophenecarbaldehyde is used as a versatile building block in organic chemistry for its capacity to serve as a precursor to a wide array of derivatives, enabling the creation of compounds with different functional groups and applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-Bromo-5-methyl-2-thiophenecarbaldehyde is used for its potential biological activity, particularly as an antimicrobial or antifungal agent, offering new avenues for the development of treatments against infectious diseases.

Upstream product

• 554-14-3 2-Methylthiophene 
• 29421-73-6 3,5-dibromo-2-methylthiophene 
• 68-12-2 N,N-dimethyl-formamide 
• 13679-70-4 5-methylthiophene-2-carboxaldehyde 

Downstream Products

• 1315330-93-8 3-(4-bromo-5-methyl-thien-2-yl)-2-cyanoacrylic acid 
• 1315330-95-0 3-[4-(4-aminophenyl)-5-methyl-thien-2-yl]-2-cyanoacrylic acid 
• 1315330-98-3 N-(2,6-diisopropylphenyl)-N'-{4-[2-methyl-5-(cyanoacrylic acid)-3-thienyl]-phenyl}-1,7-bis(6-undecanoxy)perylene-3,4,9,10-tetracarboxylic diimide 
• 1195623-96-1 5-methyl-4-bromo-2-thiopheneformaldehyde diethyl acetal 
• 1207954-31-1 (S)-4-(1-{[2-methyl-4-(4-trifluoromethylbenzyl)-4H-thieno[3,2-b]pyrrole-3-carbonyl]-amino}-ethyl)-benzoic acid 

Relevant articles and documents

Gating charge recombination rates through dynamic bridges in tetrathiafulvalene-fullerene architectures

An open and shut case: The competition between charge separation and recombination in artificial photosynthetic systems can be controlled by using photochromic dynamic bridge. The photoinduced opening and closing of the bridge mediates the electronic coupling between donor (D) and acceptor (A). Copyright

NOVEL COMPOUNDS HAVING INHIBITORY ACTIVITY ON PROSTAGLANDIN E2 RECEPTOR AND USES THEREOF

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Development of High-Performance Pyrimidine Nucleoside and Oligonucleotide Diarylethene Photoswitches

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Diarylethene compound, preparation and applications thereof

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