109179-31-9

Basic information

• Product Name: 2-Bromo-3-methylbenzaldehyde
• Synonyms: 2-Bromo-3-methylbenzaldehyde;Benzaldehyde, 2-bromo-3-methyl-
• CAS NO: 109179-31-9
• Molecular Formula: C₈H₇BrO
• Molecular Weight: 199.04458
• Mol File: 109179-31-9.mol
• Article Data: 12

Chemical Properties

• Melting Point: 53-54 °C
• Boiling Point: 250.1±20.0 °C(Predicted)
• Appearance: /
• Density: 1.490±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 2-Bromo-3-methylbenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromo-3-methylbenzaldehyde(109179-31-9)
• EPA Substance Registry System: 2-Bromo-3-methylbenzaldehyde(109179-31-9)

Safety Data

• Hazardous Substances Data: 109179-31-9(Hazardous Substances Data)

Usage

General Description

2-Bromo-3-methylbenzaldehyde is a chemical compound containing a benzene ring with a methyl group and an aldehyde functional group, as well as a bromine atom located on the 2-position of the benzene ring. 2-Bromo-3-methylbenzaldehyde is commonly used in organic synthesis for the production of various pharmaceuticals, agrochemicals, and other fine chemicals. It is also a versatile building block for the synthesis of complex organic molecules. Additionally, 2-Bromo-3-methylbenzaldehyde has been studied for its potential biological activities, including its antimicrobial, antifungal, and anticancer properties. However, it is important to handle this compound with care as it is considered to be hazardous and should be used in a controlled laboratory setting.

Upstream product

• 263159-64-4 2-bromo-3-methyl-benzonitrile 
• 52780-15-1 3'-bromo-2'-methylbenzonitrile 
• 53663-39-1 3-methyl-2-bromobenzoic acid 
• 168886-97-3 (2-bromo-3-methylphenyl)methanol 
• 131001-86-0 methyl 2-bromo-3-methylbenzoate 
• 576-22-7 2-Bromo-m-xylene 
• 66790-58-7 2-bromo-1-(bromomethyl)-3-methylbenzene 

Downstream Products

• 1101881-91-7 1-(2-bromo-3-methylphenyl)ethanol 
• 1393359-74-4 C₁₅H₁₄BrN 
• 1389315-83-6 3-methyl-2-(phenylethynyl)benzaldehyde 
• 1389315-67-6 2-benzyl-4-bromo-5-methyl-3-phenylisoquinolin-1(2H)-one 
• 1383673-48-0 1,2-bis(2-bromo-3-methylphenyl)ethene 
• 1257630-07-1 3-methyl-2-(naphthalen-1-yl)benzaldehyde 

Relevant articles and documents

An Industrial Perspective on Counter Anions in Gold Catalysis: On Alternative Counter Anions

A comparison of versatile counter anions was investigated by means of a variety of well-known test reactions representing the key reactivity patterns of homogeneous gold catalysis, the catalytic activity was monitored by GC and 1H NMR. As previ

Selective Oxidation of 2-Bromo-m-xylene to 2-Bromo-3-methylbenzoic Acid or 2-Bromoisophthalic Acid

Aqueous sodium dichromate oxidation of 2-bromo-m-xylene (1) under a carbon dioxide pressure gave 2-bromoisophthalic acid (58percent), while NBS-bromination of 1 followed by Sommelet oxidation to aldehyde and then potassium permanganate oxidation enabled t

5-MEMBERED HETEROARYLAMINOSULFONAMIDES FOR TREATING CONDITIONS MEDIATED BY DEFICIENT CFTR ACTIVITY

The invention relates to heteroaryl compounds, pharmaceutically acceptable salts thereof, and pharmaceutical preparations thereof. Also described herein are compositions and the use of such compounds in methods of treating diseases and conditions mediated by deficient CFTR activity, in particular cystic fibrosis.

An Industrial Perspective on Counter Anions in Gold Catalysis: Underestimated with Respect to “Ligand Effects”

The conversion of a variety of well-known test reactions, representing the key reactivity patterns of gold catalysis, were analyzed by GC and 1H NMR. The study is focused on establishing of a strategical approach for the consideration of ligand