2-Amino-2-(2-bromophenyl)acetic acid

98%

Reagent Code: #138090
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CAS Number 254762-66-8

science Other reagents with same CAS 254762-66-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.06 g/mol
Formula C₈H₈BrNO₂
badge Registry Numbers
MDL Number MFCD02662413
thermostat Physical Properties
Boiling Point 351 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structure allows incorporation into more complex molecules that exhibit biological activity, such as anticonvulsant or anxiolytic effects. The bromophenyl group enables further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for drug design and optimization. Also utilized in the preparation of analogs for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,740.00
inventory 1g
10-20 days ฿4,920.00
inventory 5g
10-20 days ฿20,050.00

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2-Amino-2-(2-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. Its structure allows incorporation into more complex molecules that exhibit biological activity, such as anticonvulsant or anxiolytic effects. The bromophenyl group enables further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for drug design and optimization. Also utilized in the preparation of analogs for structure-activity rel

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structure allows incorporation into more complex molecules that exhibit biological activity, such as anticonvulsant or anxiolytic effects. The bromophenyl group enables further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for drug design and optimization. Also utilized in the preparation of analogs for structure-activity relationship studies.

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