(R)-Methyl 2-amino-3-(3-fluorophenyl)propanoate hydrochloride

98%

Reagent Code: #228584
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CAS Number 201479-09-6

science Other reagents with same CAS 201479-09-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.67 g/mol
Formula C₁₀H₁₃ClFNO₂
badge Registry Numbers
MDL Number MFCD00672371
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its fluorinated phenyl group and chiral amine functionality make it valuable for constructing active ingredients in antidepressants and anticonvulsants. The compound’s stereochemistry allows for selective interaction with biological targets, improving drug efficacy and reducing side effects. It is also employed in the preparation of protease inhibitors and other bioactive molecules where enantiomeric purity is critical. Commonly utilized in research and process chemistry for route optimization in API manufacturing.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,780.00
inventory 1g
10-20 days ฿11,600.00
inventory 5g
10-20 days ฿56,000.00
(R)-Methyl 2-amino-3-(3-fluorophenyl)propanoate hydrochloride
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its fluorinated phenyl group and chiral amine functionality make it valuable for constructing active ingredients in antidepressants and anticonvulsants. The compound’s stereochemistry allows for selective interaction with biological targets, improving drug efficacy and reducing side effects. It is also employed in the preparation of protease inhibitors and ot

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its fluorinated phenyl group and chiral amine functionality make it valuable for constructing active ingredients in antidepressants and anticonvulsants. The compound’s stereochemistry allows for selective interaction with biological targets, improving drug efficacy and reducing side effects. It is also employed in the preparation of protease inhibitors and other bioactive molecules where enantiomeric purity is critical. Commonly utilized in research and process chemistry for route optimization in API manufacturing.

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