2-amino-2-(3-bromophenyl)acetic acid

95%

Reagent Code: #135174
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CAS Number 79422-73-4

science Other reagents with same CAS 79422-73-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.06 g/mol
Formula C₈H₈BrNO₂
badge Registry Numbers
MDL Number MFCD00665358
thermostat Physical Properties
Melting Point 212-215 °C
Boiling Point 351.6 °C at 760 mmHg
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 central nervous system agents and anticonvulsant drugs. Its structure allows for incorporation into more complex molecules where the bromophenyl and amino acid functionalities are essential for biological activity. Also employed in the preparation of analogs for structure-activity relationship (SAR) studies in medicinal chemistry. The presence of both amine and carboxylic acid groups makes it suitable for peptide coupling reactions, enabling its use in designing bioactive peptides. Additionally, it serves as a building block in combinatorial chemistry for drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,560.00
inventory 1g
10-20 days ฿6,130.00
inventory 5g
10-20 days ฿20,310.00
inventory 25g
10-20 days ฿81,970.00

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2-amino-2-(3-bromophenyl)acetic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and anticonvulsant drugs. Its structure allows for incorporation into more complex molecules where the bromophenyl and amino acid functionalities are essential for biological activity. Also employed in the preparation of analogs for structure-activity relationship (SAR) studies in medicinal chemistry. The presence of both amine and carboxylic acid groups makes it suitable for p

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and anticonvulsant drugs. Its structure allows for incorporation into more complex molecules where the bromophenyl and amino acid functionalities are essential for biological activity. Also employed in the preparation of analogs for structure-activity relationship (SAR) studies in medicinal chemistry. The presence of both amine and carboxylic acid groups makes it suitable for peptide coupling reactions, enabling its use in designing bioactive peptides. Additionally, it serves as a building block in combinatorial chemistry for drug discovery.

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