METHYL (R)-3-([1,1'-BIPHENYL]-4-YL)-2-AMINOPROPANOATE HYDROCHLORIDE

98%

Reagent Code: #214490
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CAS Number 169885-19-2

science Other reagents with same CAS 169885-19-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.77 g/mol
Formula C₁₆H₁₈ClNO₂
badge Registry Numbers
MDL Number MFCD24434458
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors such as those used in antiviral therapies. It serves as a chiral building block in asymmetric synthesis, enabling the production of enantiomerically pure compounds. Its ester and amine functionalities allow for peptide coupling and further functionalization, making it valuable in medicinal chemistry for drug discovery and optimization. Commonly employed in the preparation of beta-amino acid derivatives and used in research settings for designing enzyme inhibitors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,230.00

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METHYL (R)-3-([1,1'-BIPHENYL]-4-YL)-2-AMINOPROPANOATE HYDROCHLORIDE
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors such as those used in antiviral therapies. It serves as a chiral building block in asymmetric synthesis, enabling the production of enantiomerically pure compounds. Its ester and amine functionalities allow for peptide coupling and further functionalization, making it valuable in medicinal chemistry for drug discovery and optimization. Commonly employed in the preparation of beta-amino acid deriv

Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors such as those used in antiviral therapies. It serves as a chiral building block in asymmetric synthesis, enabling the production of enantiomerically pure compounds. Its ester and amine functionalities allow for peptide coupling and further functionalization, making it valuable in medicinal chemistry for drug discovery and optimization. Commonly employed in the preparation of beta-amino acid derivatives and used in research settings for designing enzyme inhibitors.

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