(R)-tert-Butyl 2-amino-3-(3-bromophenyl)propanoate hydrochloride

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Reagent Code: #55959
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CAS Number 1956436-14-8

science Other reagents with same CAS 1956436-14-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 336.65 g/mol
Formula C₁₃H₁₉BrClNO₂
badge Registry Numbers
MDL Number MFCD30063282
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This chemical is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various bioactive compounds. Its structure, featuring a bromophenyl group and an amino ester, makes it valuable for constructing molecules with potential therapeutic applications, particularly in the design of drugs targeting neurological disorders or as part of peptide mimetics. The chiral center allows for the creation of enantiomerically pure compounds, which is crucial for optimizing drug efficacy and reducing side effects. Additionally, it may be employed in organic synthesis to explore new chemical reactions or pathways, contributing to advancements in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,188.00
inventory 250mg
10-20 days ฿2,025.00
inventory 1g
10-20 days ฿5,481.00

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(R)-tert-Butyl 2-amino-3-(3-bromophenyl)propanoate hydrochloride
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This chemical is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various bioactive compounds. Its structure, featuring a bromophenyl group and an amino ester, makes it valuable for constructing molecules with potential therapeutic applications, particularly in the design of drugs targeting neurological disorders or as part of peptide mimetics. The chiral center allows for the creation of enantiomerically pure compounds,

This chemical is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various bioactive compounds. Its structure, featuring a bromophenyl group and an amino ester, makes it valuable for constructing molecules with potential therapeutic applications, particularly in the design of drugs targeting neurological disorders or as part of peptide mimetics. The chiral center allows for the creation of enantiomerically pure compounds, which is crucial for optimizing drug efficacy and reducing side effects. Additionally, it may be employed in organic synthesis to explore new chemical reactions or pathways, contributing to advancements in medicinal chemistry.

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