(S)-2-(2-Bromophenyl)-2-((tert-butoxycarbonyl)amino)acetic acid

≥95%

Reagent Code: #38621
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CAS Number 1228547-87-2

science Other reagents with same CAS 1228547-87-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 330.17 g/mol
Formula C₁₃H₁₆BrNO₄
badge Registry Numbers
MDL Number MFCD07371725
thermostat Physical Properties
Boiling Point 456.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the production of chiral compounds, where its stereochemistry plays a crucial role in ensuring the desired biological activity of the final product. The tert-butoxycarbonyl (Boc) protecting group allows for selective reactions to occur at other functional sites, making it valuable in peptide synthesis and the development of active pharmaceutical ingredients (APIs). Its bromophenyl moiety can also be leveraged in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to construct more elaborate structures. Overall, it is a versatile building block in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,368.00
inventory 250mg
10-20 days ฿20,745.00

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(S)-2-(2-Bromophenyl)-2-((tert-butoxycarbonyl)amino)acetic acid
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This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the production of chiral compounds, where its stereochemistry plays a crucial role in ensuring the desired biological activity of the final product. The tert-butoxycarbonyl (Boc) protecting group allows for selective reactions to occur at other functional sites, making it valuable in peptide synthesis and the development of active pharmaceutical in

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the production of chiral compounds, where its stereochemistry plays a crucial role in ensuring the desired biological activity of the final product. The tert-butoxycarbonyl (Boc) protecting group allows for selective reactions to occur at other functional sites, making it valuable in peptide synthesis and the development of active pharmaceutical ingredients (APIs). Its bromophenyl moiety can also be leveraged in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to construct more elaborate structures. Overall, it is a versatile building block in medicinal chemistry and drug discovery.

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