75097-32-4

Basic information

• Product Name: (2-bromo-5-methoxy-4-methylphenyl)acetic acid
• CAS NO: 75097-32-4
• Molecular Formula: C₁₀H₁₁BrO₃
• Molecular Weight: 259.0965
• Mol File: 75097-32-4.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 368.7°C at 760 mmHg
• Flash Point: 176.8°C
• Density: 1.494g/cm³
• Vapor Pressure: 4.37E-06mmHg at 25°C
• Refractive Index: 1.566
• CAS DataBase Reference: (2-bromo-5-methoxy-4-methylphenyl)acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (2-bromo-5-methoxy-4-methylphenyl)acetic acid(75097-32-4)
• EPA Substance Registry System: (2-bromo-5-methoxy-4-methylphenyl)acetic acid(75097-32-4)

Safety Data

• Hazardous Substances Data: 75097-32-4(Hazardous Substances Data)

Usage

Description

(2-bromo-5-methoxy-4-methylphenyl)acetic acid is a chemical compound with the molecular formula C10H11BrO3. It is a derivative of acetic acid, featuring a bromine atom, a methoxy group, and a methyl group attached to a benzene ring. (2-bromo-5-methoxy-4-methylphenyl)acetic acid has potential applications in the pharmaceutical industry due to its structural features and potential biological activities. It may also serve as a building block in organic synthesis for creating more complex compounds. Careful handling and adherence to safety protocols are essential when working with this compound, as it may have potential hazards associated with its use.

Uses

Used in Pharmaceutical Industry:
(2-bromo-5-methoxy-4-methylphenyl)acetic acid is used as a pharmaceutical intermediate for the development of new drugs, leveraging its unique structural features and potential biological activities to target specific therapeutic areas.
Used in Organic Synthesis:
(2-bromo-5-methoxy-4-methylphenyl)acetic acid is used as a building block in organic synthesis to create more complex compounds, contributing to the advancement of chemical research and the development of novel materials and pharmaceuticals.

Upstream product

• 57335-02-1 2-bromo-5-methoxy-4-methylphenylacetonitrile 
• 57295-30-4 3-hydroxy-4-methylbenzaldehyde 
• 24973-22-6 3-methoxy-4-methylbenzaldehyde 
• 4685-50-1 3-methoxy-4-methylbenzyl alcohol 
• 64829-31-8 2-(3-methoxy-4-methylphenyl)acetonitrile 
• 100861-38-9 (3-methoxy-4-methylphenyl)acetic acid 

Downstream Products

• 75156-81-9 methyl α-bromo-(2-bromo-5-methoxy-4-methylphenyl)acetate 
• 75156-82-0 methyl α-bromo-(2-bromo-5-methoxy-4-methoxymethylphenyl)acetate 
• 75097-36-8 benzyl 2, 3, 3a, 4, 10a, 10b-hexahydro-8-methoxy-3,7,-dimethyl-2-oxo-10H-oxazolo<4', 5'-3, 4>pyrrolo<1,2-a>indole-10-carboxylate 
• 75097-35-7 (+/-)-benzyl 1α-acetoxy-2β-(N-ethoxycarbonyl-N-methylamino)2,3-dihydro-7-methoxy-6-methyl-1H-pyrrolo<1,2-a>indole-9-carboxylate 
• 75097-34-6 benzyl (Z)-α-<3-acetoxy-4-(N-ethoxycarbonyl-N-methylamino)pyrrolidin-2-ylidene>-α-(2-bromo-5-methoxy-4-methylphenyl)acetate 
• 75156-86-4 methyl α-<3-acetoxy-4-(N-ethoxycarbonyl-N-methylamino)-pyrrolidin-2-ylidene>-α-(2-bromo-5-methoxy-4-methoxymethylphenyl)-acetate 
• 1232402-52-6 (2-bromo-5-methoxy-4-methyl-phenyl)-acetic acid chloride 

Relevant articles and documents

DIHYDROPYRIDONE AMIDES AS P2X7 MODULATORS

Compounds of the formula I: or pharmaceutically acceptable salts thereof, wherein m, n, R1, R2, R3, R4 and R5 are as defined herein. Also disclosed are methods of making the compounds and using the compounds for treatment of diseases associated with the P2X7 purinergic receptor.