(S)-3-(4-Boronophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid

98%

Reagent Code: #57157
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CAS Number 119771-23-2

science Other reagents with same CAS 119771-23-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 309.12 g/mol
Formula C₁₄H₂₀BNO₆
badge Registry Numbers
MDL Number MFCD01860642
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily used in the field of medicinal chemistry and drug development, particularly in the synthesis of boron-containing compounds. Its boronic acid functional group makes it valuable in the design of protease inhibitors, which are crucial in treating diseases like cancer, HIV, and hypertension. The compound is also employed in Suzuki-Miyaura cross-coupling reactions, a widely used method in organic synthesis to create complex molecules for pharmaceuticals. Additionally, its tert-butoxycarbonyl (Boc) protecting group allows for selective reactions, making it a versatile intermediate in peptide synthesis. Its applications extend to the development of boron neutron capture therapy (BNCT) agents, a targeted cancer treatment approach.

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Test Parameter Specification
Appearance White to Light yellow Solid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿10,035.00
inventory 1g
10-20 days ฿909.00
inventory 5g
10-20 days ฿2,781.00

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(S)-3-(4-Boronophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid
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This chemical is primarily used in the field of medicinal chemistry and drug development, particularly in the synthesis of boron-containing compounds. Its boronic acid functional group makes it valuable in the design of protease inhibitors, which are crucial in treating diseases like cancer, HIV, and hypertension. The compound is also employed in Suzuki-Miyaura cross-coupling reactions, a widely used method in organic synthesis to create complex molecules for pharmaceuticals. Additionally, its tert-butox

This chemical is primarily used in the field of medicinal chemistry and drug development, particularly in the synthesis of boron-containing compounds. Its boronic acid functional group makes it valuable in the design of protease inhibitors, which are crucial in treating diseases like cancer, HIV, and hypertension. The compound is also employed in Suzuki-Miyaura cross-coupling reactions, a widely used method in organic synthesis to create complex molecules for pharmaceuticals. Additionally, its tert-butoxycarbonyl (Boc) protecting group allows for selective reactions, making it a versatile intermediate in peptide synthesis. Its applications extend to the development of boron neutron capture therapy (BNCT) agents, a targeted cancer treatment approach.

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