(S)-Methyl 2-amino-3-cyclopentylpropanoate hydrochloride

98%

Reagent Code: #233288
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CAS Number 1191996-99-2

science Other reagents with same CAS 1191996-99-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.7 g/mol
Formula C₉H₁₈ClNO₂
badge Registry Numbers
MDL Number MFCD22494959
thermostat Physical Properties
Boiling Point 791.1±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.400±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its cyclopentyl and amino ester functionalities make it valuable for constructing biologically active molecules with high stereoselectivity. Commonly employed in the preparation of hepatitis C virus (HCV) NS3/4A protease inhibitors due to its ability to mimic natural amino acid substrates. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug potency and metabolic stability.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿23,750.00

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(S)-Methyl 2-amino-3-cyclopentylpropanoate hydrochloride
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its cyclopentyl and amino ester functionalities make it valuable for constructing biologically active molecules with high stereoselectivity. Commonly employed in the preparation of hepatitis C virus (HCV) NS3/4A protease inhibitors due to its ability to mimic natural amino acid substrates. Also utilized in medicinal chemistry for structure-activity relat

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its cyclopentyl and amino ester functionalities make it valuable for constructing biologically active molecules with high stereoselectivity. Commonly employed in the preparation of hepatitis C virus (HCV) NS3/4A protease inhibitors due to its ability to mimic natural amino acid substrates. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug potency and metabolic stability.

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