2-Bromo-5-hydroxy-4-methoxybenzoic acid

95%

Reagent Code: #148269
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CAS Number 121936-68-3

science Other reagents with same CAS 121936-68-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.04 g/mol
Formula C₈H₇BrO₄
badge Registry Numbers
MDL Number MFCD16659606
thermostat Physical Properties
Boiling Point 367°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of bioactive compounds. Its functional groups—bromo, hydroxy, methoxy, and carboxylic acid—allow for selective chemical modifications, making it valuable in constructing complex organic molecules. Commonly employed in coupling reactions and heterocycle formation, it plays a role in creating drug candidates with potential antimicrobial, anti-inflammatory, or anticancer activity. Also utilized in research settings for the design of novel organic materials and enzyme inhibitors.

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Test Parameter Specification
Appearance Off-white to gray solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿126.50
inventory 25g
10-20 days ฿313.50
inventory 100g
10-20 days ฿935.00

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2-Bromo-5-hydroxy-4-methoxybenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of bioactive compounds. Its functional groups—bromo, hydroxy, methoxy, and carboxylic acid—allow for selective chemical modifications, making it valuable in constructing complex organic molecules. Commonly employed in coupling reactions and heterocycle formation, it plays a role in creating drug candidates with potential antimicrobial, anti-inflammatory, or anticancer activity. Also utilized in re
Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of bioactive compounds. Its functional groups—bromo, hydroxy, methoxy, and carboxylic acid—allow for selective chemical modifications, making it valuable in constructing complex organic molecules. Commonly employed in coupling reactions and heterocycle formation, it plays a role in creating drug candidates with potential antimicrobial, anti-inflammatory, or anticancer activity. Also utilized in research settings for the design of novel organic materials and enzyme inhibitors.
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