(S)-()-2-Amino-4-bromobutyric acid hydrobromide

98%

Reagent Code: #234208
label
Alias L(+)-2-amino-4-bromobutyrate hydrobromide
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CAS Number 15159-65-6

science Other reagents with same CAS 15159-65-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.93 g/mol
Formula BrCH₂CH₂CH(NH₂)CO₂H·HBr
badge Registry Numbers
MDL Number MFCD01631290
thermostat Physical Properties
Melting Point 189 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of neuroactive compounds and enzyme inhibitors. Its bromine functionality allows for further chemical modifications through cross-coupling reactions. Commonly employed in research settings for the preparation of gamma-aminobutyric acid (GABA) analogs due to its structural similarity. Also utilized in asymmetric synthesis where the chiral amine center serves as a directing group or intermediate in complex molecule construction.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿2,000.00
inventory 1g
10-20 days ฿2,964.50

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(S)-()-2-Amino-4-bromobutyric acid hydrobromide
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of neuroactive compounds and enzyme inhibitors. Its bromine functionality allows for further chemical modifications through cross-coupling reactions. Commonly employed in research settings for the preparation of gamma-aminobutyric acid (GABA) analogs due to its structural similarity. Also utilized in asymmetric synthesis where the chiral amine center serves as a directing group or intermediate in complex

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of neuroactive compounds and enzyme inhibitors. Its bromine functionality allows for further chemical modifications through cross-coupling reactions. Commonly employed in research settings for the preparation of gamma-aminobutyric acid (GABA) analogs due to its structural similarity. Also utilized in asymmetric synthesis where the chiral amine center serves as a directing group or intermediate in complex molecule construction.

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