(1S,2R,4S)-N-BOC-1-AMINO-2-HYDROXYCYCLOPENTANE-4-CARBOXYLIC ACID METHYL ESTER

97%

Reagent Code: #232516
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CAS Number 321744-21-2

science Other reagents with same CAS 321744-21-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.2988 g/mol
Formula C₁₂H₂₁NO₅
badge Registry Numbers
MDL Number MFCD02259723
thermostat Physical Properties
Boiling Point 402.56 °C(rough estimate)
inventory_2 Storage & Handling
Density 1.1623 g/cm3(rough estimate)
Storage 2-8°C

description Product Description

Widely used in pharmaceutical synthesis, this compound serves as a chiral building block for the preparation of biologically active molecules, particularly protease inhibitors and antiviral agents. Its protected amine and esterified carboxyl group allow for selective reactions in multi-step organic syntheses. The hydroxyl and carboxylic ester functionalities, along with defined stereochemistry, make it valuable for constructing cyclic scaffolds found in enzyme inhibitors. It is especially useful in medicinal chemistry for developing drugs targeting viral replication and metabolic disorders.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,190.00
inventory 500mg
10-20 days ฿39,600.00
(1S,2R,4S)-N-BOC-1-AMINO-2-HYDROXYCYCLOPENTANE-4-CARBOXYLIC ACID METHYL ESTER
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Widely used in pharmaceutical synthesis, this compound serves as a chiral building block for the preparation of biologically active molecules, particularly protease inhibitors and antiviral agents. Its protected amine and esterified carboxyl group allow for selective reactions in multi-step organic syntheses. The hydroxyl and carboxylic ester functionalities, along with defined stereochemistry, make it valuable for constructing cyclic scaffolds found in enzyme inhibitors. It is especially useful in medic

Widely used in pharmaceutical synthesis, this compound serves as a chiral building block for the preparation of biologically active molecules, particularly protease inhibitors and antiviral agents. Its protected amine and esterified carboxyl group allow for selective reactions in multi-step organic syntheses. The hydroxyl and carboxylic ester functionalities, along with defined stereochemistry, make it valuable for constructing cyclic scaffolds found in enzyme inhibitors. It is especially useful in medicinal chemistry for developing drugs targeting viral replication and metabolic disorders.

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