2-Amino-6-bromobenzoic acid

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Reagent Code: #134974
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CAS Number 20776-48-1

science Other reagents with same CAS 20776-48-1

blur_circular Chemical Specifications

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Weight 216.03 g/mol
Formula C₇H₆BrNO₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive compounds. It serves as a building block in organic synthesis due to the presence of both amino and carboxylic acid functional groups, allowing for peptide coupling and heterocycle formation. Also employed in the preparation of dyes and agrochemicals where brominated aromatic scaffolds are required. Its structure supports further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿156.00
inventory 5g
10-20 days ฿860.00
inventory 25g
10-20 days ฿4,100.00
inventory 100g
10-20 days ฿16,260.00

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2-Amino-6-bromobenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive compounds. It serves as a building block in organic synthesis due to the presence of both amino and carboxylic acid functional groups, allowing for peptide coupling and heterocycle formation. Also employed in the preparation of dyes and agrochemicals where brominated aromatic scaffolds are required. Its structure supports further functionalizati

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive compounds. It serves as a building block in organic synthesis due to the presence of both amino and carboxylic acid functional groups, allowing for peptide coupling and heterocycle formation. Also employed in the preparation of dyes and agrochemicals where brominated aromatic scaffolds are required. Its structure supports further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry research.

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