5-Bromo-3-hydroxy-2-methylbenzoic acid

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Reagent Code: #156399
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CAS Number 1442643-22-2

science Other reagents with same CAS 1442643-22-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.04 g/mol
Formula C₈H₇BrO₃
badge Registry Numbers
MDL Number MFCD28142846
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—bromine, hydroxyl, and carboxylic acid—allow for selective chemical modifications, enabling coupling reactions, derivatization, and ring transformations. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its aromatic scaffold and ease of substitution. Also utilized in the preparation of agrochemicals and specialty polymers where halogenated aromatic acids enhance stability and reactivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,130.00
inventory 250mg
10-20 days ฿7,000.00

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5-Bromo-3-hydroxy-2-methylbenzoic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—bromine, hydroxyl, and carboxylic acid—allow for selective chemical modifications, enabling coupling reactions, derivatization, and ring transformations. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its aromatic scaffold and ease of substitution. Also utiliz

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—bromine, hydroxyl, and carboxylic acid—allow for selective chemical modifications, enabling coupling reactions, derivatization, and ring transformations. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its aromatic scaffold and ease of substitution. Also utilized in the preparation of agrochemicals and specialty polymers where halogenated aromatic acids enhance stability and reactivity.

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