Methyl (2S,4S)-1-Boc-4-aminopyrrolidine-2-carboxylate

≥95%

Reagent Code: #76150
fingerprint
CAS Number 121148-01-4

science Other reagents with same CAS 121148-01-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.29 g/mol
Formula C₁₁H₂₀N₂O₄
badge Registry Numbers
MDL Number MFCD01861781
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is widely used in the synthesis of pharmaceuticals, particularly in the development of peptidomimetics and protease inhibitors. Its structure, featuring both a Boc-protected amine and a carboxylate ester, makes it a versatile intermediate in organic synthesis. It is often employed in the construction of complex molecules, especially in the field of medicinal chemistry, where it serves as a building block for creating biologically active compounds. The stereochemistry of the molecule is crucial for its application in enantioselective synthesis, ensuring the production of specific stereoisomers with desired biological activity. Additionally, it is utilized in the preparation of chiral ligands and catalysts, which are essential in asymmetric synthesis.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Colorless to yellow liquid
Purity 95-100%
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿55,760.00
inventory 1g
10-20 days ฿16,310.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Methyl (2S,4S)-1-Boc-4-aminopyrrolidine-2-carboxylate
No image available
This compound is widely used in the synthesis of pharmaceuticals, particularly in the development of peptidomimetics and protease inhibitors. Its structure, featuring both a Boc-protected amine and a carboxylate ester, makes it a versatile intermediate in organic synthesis. It is often employed in the construction of complex molecules, especially in the field of medicinal chemistry, where it serves as a building block for creating biologically active compounds. The stereochemistry of the molecule is crucial for its application in enantioselective synthesis, ensuring the production of specific stereoisomers with desired biological activity. Additionally, it is utilized in the preparation of chiral ligands and catalysts, which are essential in asymmetric synthesis.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...