854646-94-9

Basic information

• Product Name: 2-(5-BroMo-2-Methylphenyl)acetic acid
• Synonyms: 2-(5-BroMo-2-Methylphenyl)acetic acid;(5-Bromo-2-methylphenyl)acetic acid;5-Bromo-2-methylbenzeneacetic acid
• CAS NO: 854646-94-9
• Molecular Formula: C9H9BrO2
• Molecular Weight: 229.07056
• Mol File: 854646-94-9.mol
• Article Data: 5

Chemical Properties

• Melting Point: 93.5-94.5 °C
• Boiling Point: 344.7±27.0 °C(Predicted)
• Appearance: /
• Density: 1.533±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 4.13±0.10(Predicted)
• CAS DataBase Reference: 2-(5-BroMo-2-Methylphenyl)acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(5-BroMo-2-Methylphenyl)acetic acid(854646-94-9)
• EPA Substance Registry System: 2-(5-BroMo-2-Methylphenyl)acetic acid(854646-94-9)

Safety Data

• Hazardous Substances Data: 854646-94-9(Hazardous Substances Data)

Usage

General Description

2-(5-Bromo-2-Methylphenyl)acetic acid is a chemical compound with the molecular formula C9H9BrO2. It is commonly used as an intermediate in the synthesis of pharmaceuticals and organic compounds. 2-(5-BroMo-2-Methylphenyl)acetic acid is a derivative of acetic acid with a bromine and a methyl group attached to a phenyl ring. It is known to exhibit anti-inflammatory and analgesic properties and has been studied for its potential therapeutic applications. The chemical structure and properties of 2-(5-Bromo-2-Methylphenyl)acetic acid make it a valuable and versatile compound in the field of organic chemistry and pharmaceutical research.

Upstream product

• 50-00-0 formaldehyd 
• 106-38-7 para-bromotoluene 
• 880134-34-9 (5-iodo-2-methylphenyl)-acetic acid methyl ester 
• 873-75-6 4-bromobenzenemethanol 
• 87604-18-0 4-bromo-2-(chloromethyl)-1-methylbenzene 
• 79669-49-1 5-bromo-2-methylbenzoic acid 
• 1231244-85-1 2-(5-bromo-2-methylphenyl)acetonitrile 
• 258886-04-3 (5-bromo-2-methylphenyl)methanol 
• 258886-05-4 5-bromo-2-methylbenzyl bromide 

Relevant articles and documents

AMINE OR (THIO)AMIDE CONTAINING LXR MODULATORS

The present invention relates to derivatives of formula (I) which bind to the liver X receptor (LXRα and/or LXRβ) and act preferably as inverse agonists of LXR.

Aromatic Claisen Rearrangements of Benzyl Ketene Acetals: Conversion of Benzylic Alcohols to (ortho-Tolyl)acetates

Claisen rearrangements of benzyl vinyl ethers are much less facile than those of aliphatic allyl vinyl ethers, and their synthetic utility has remained relatively unexplored. A one-pot procedure is reported for the generation and Claisen rearrangement of benzyl vinyl ethers that contain an activating α-alkoxy substituent on the vinyl group. A [3,3]-sigmatropic mechanism was supported by trapping of the intermediate isotoluene in an intramolecular Alder–ene reaction.

IODINE-PHENYL-SUBSTITUTED CYCLIC CETOENOLS

The invention relates to novel iodine-phenyl-substituted cyclic cetoenols of formula (I) wherein CKE, J, X and Y have the above-mentioned meanings, several methods and intermediate products for the production thereof and the use thereof as pesticide agents and/or herbicides which contain iodine-phenyl-substituted cyclic cetoenols of formula (I) and at least one compound which improves the compatibility of cultivated plants.