3-AMINO-3-(3-BROMOPHENYL)PROPIONIC ACID

95%

Reagent Code: #135424
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CAS Number 117391-50-1

science Other reagents with same CAS 117391-50-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.09 g/mol
Formula C₉H₁₀BrNO₂
badge Registry Numbers
MDL Number MFCD00995843
thermostat Physical Properties
Melting Point 227°C dec. (Lit.)
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 analgesic compounds. Its structure allows for the formation of bioactive molecules through modification of both the amino and carboxylic acid functional groups. Commonly employed in research settings for designing GABA analogs and studying receptor binding due to its aryl-substituted beta-amino acid framework. Also utilized in the preparation of enzyme inhibitors and as a building block in medicinal chemistry for creating peptidomimetics with enhanced metabolic stability.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 225-229
Purity 94.5-100
Appearance SOLID

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿174.00
5g
10-20 days ฿960.00
25g
10-20 days ฿4,570.00
3-AMINO-3-(3-BROMOPHENYL)PROPIONIC 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 analgesic compounds. Its structure allows for the formation of bioactive molecules through modification of both the amino and carboxylic acid functional groups. Commonly employed in research settings for designing GABA analogs and studying receptor binding due to its aryl-substituted beta-amino acid framework. Also utilized in the preparation of enzyme inhibitors and as a b

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and analgesic compounds. Its structure allows for the formation of bioactive molecules through modification of both the amino and carboxylic acid functional groups. Commonly employed in research settings for designing GABA analogs and studying receptor binding due to its aryl-substituted beta-amino acid framework. Also utilized in the preparation of enzyme inhibitors and as a building block in medicinal chemistry for creating peptidomimetics with enhanced metabolic stability.

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