189331-47-3

Basic information

• Product Name: 2-BROMO-3-METHYL-5-FORMYLTHIOPHENE
• Synonyms: 2-BROMO-3-METHYL-5-FORMYLTHIOPHENE;5-bromo-4-methylthiophene-2-carbaldehyde;5-Bromo-4-methylthiophene-2-carboxaldehyde 99%;2-Bromo-3-methylthiophene-5-carboxaldehyde, 2-Bromo-5-formyl-3-methylthiophene;2-broMo-3-hexyl -5-forMylthiophene;5-Bromo-4-methylthiophene-2-carboxaldehyde
• CAS NO: 189331-47-3
• Molecular Formula: C₆H₅BrOS
• Molecular Weight: 205.07
• EINECS: 604-604-1
• Product Categories: Building Blocks;Thiophene
• Mol File: 189331-47-3.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 264.996 °C at 760 mmHg
• Flash Point: 114.066 °C
• Appearance: /
• Density: 1.667 g/cm³
• Vapor Pressure: 0.009mmHg at 25°C
• Refractive Index: 1.632
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 2-BROMO-3-METHYL-5-FORMYLTHIOPHENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMO-3-METHYL-5-FORMYLTHIOPHENE(189331-47-3)
• EPA Substance Registry System: 2-BROMO-3-METHYL-5-FORMYLTHIOPHENE(189331-47-3)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 189331-47-3(Hazardous Substances Data)

Usage

General Description

2-BROMO-3-METHYL-5-FORMYLTHIOPHENE is an organic compound with the chemical formula C6H5BrOS and a molecular weight of 203.07 g/mol. It is a yellow to light brown liquid with a pungent odor. This chemical is used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. It has also been studied for its potential use as a chemical intermediate in the production of various organic compounds. 2-BROMO-3-METHYL-5-FORMYLTHIOPHENE is classified as a hazardous substance, and proper handling and storage procedures should be followed when working with this compound.

InChI:InChI=1/C6H5BrOS/c1-4-2-5(3-8)9-6(4)7/h2-3H,1H3

Upstream product

• 14282-76-9 2-bromo-3-methylthiophene 
• 616-44-4 3-Methylthiophene 
• 68-12-2 N,N-dimethyl-formamide 
• 109-89-7 diethylamine 
• 6030-36-0 4-methylthiophene-2-carbaldehyde 

Downstream Products

• 951781-88-7 2-(4-methoxyphenyl)-3-methylthiophene 
• 1254961-59-5 2-((4-methyl-5-(4-(naphthalen-1-yl(phenyl)amino)phenyl)thiophen-2-yl)methylene)malononitrile 
• 1254961-58-4 4-methyl-5-(4-(naphthalen-1-yl(phenyl)amino)phenyl)thiophene-2-carbaldehyde 
• 1254961-57-3 N-(4-(5-(5,5-dimethyl-1,3-dioxan-2-yl)-3-methylthiophen-2-yl)phenyl)-N-phenylnaphthalen-1-amine 
• 654067-69-3 5-[2-(4-diphenylaminophenyl)]-4-methylthiophene-2-carbaldehyde 
• 945392-07-4 5-bromo-4-methyl-5-(oxazol-5-yl)-thiophene 
• 54796-53-1 5-Bromo-4-methyl-thiophene-2-carboxylic acid 
• 304854-52-2 5-bromo-4-methyl-2-thiophenecarbonitrile 

Relevant articles and documents

Preparation method of non-fullerene electronic acceptor, product and application

The material adopts an aromatic or heteroaromatic fused ring to enlarge the planar π-conjugated skeleton as an arm unit, so π-electron delocalization and molecular accumulation are promoted, and the fused ring structure can promote red shift absorption as part of the planar skeleton. The π-extending conjugated structure and the fused ring nucleus rich in the thiophene structure are introduced into the star structure, so that the structure maintains the advantages of strong absorption of the linear structure, easy modification, good thermal stability, strong electron donating capacity, good rigidity and the like.

Design of potent and selective hybrid inhibitors of the mitotic kinase nek2: Structure-activity relationship, structural biology, and cellular activity

We report herein a series of Nek2 inhibitors based on an aminopyridine scaffold. These compounds have been designed by combining key elements of two previously discovered chemical series. Structure based design led to aminopyridine (R)-21, a potent and selective inhibitor able to modulate Nek2 activity in cells.

Nonvolatile memory organic field effect transistor induced by the steric hindrance effects of organic molecules

We report a nonvolatile memory organic field effect transistor (OFET) using ambipolar organic molecules as nano-interfaced semiconductor materials. Newly synthesized push-pull organic molecules (PPOMs) containing triarylamine as an electron donating group