Boc-3-(2-pyridyl)-L-alanine

98%

Reagent Code: #124909
fingerprint
CAS Number 65813-55-0

science Other reagents with same CAS 65813-55-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.2643 g/mol
Formula C₁₃H₁₆O₃
badge Registry Numbers
MDL Number MFCD08275584
thermostat Physical Properties
Boiling Point 377.952℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.107g/ml
Storage 2-8℃, dry

description Product Description

This compound is primarily used in peptide synthesis as a protected form of L-alanine. The Boc (tert-butoxycarbonyl) group safeguards the amino group during the peptide chain assembly, while the pyridyl side chain can participate in coordination chemistry or act as a ligand in metal complexes. It is particularly useful in designing peptides with specific structural or functional properties, such as those intended for biochemical studies or drug development. Additionally, the pyridyl moiety can enhance the solubility of peptides in aqueous solutions, making it valuable in creating biologically active compounds. Its application extends to research involving enzyme inhibitors, receptor ligands, and other bioactive molecules.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Off-White To Light Yellow Solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿47,520.00
inventory 5mg
10-20 days ฿13,600.00
inventory 1mg
10-20 days ฿5,680.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Boc-3-(2-pyridyl)-L-alanine
No image available
This compound is primarily used in peptide synthesis as a protected form of L-alanine. The Boc (tert-butoxycarbonyl) group safeguards the amino group during the peptide chain assembly, while the pyridyl side chain can participate in coordination chemistry or act as a ligand in metal complexes. It is particularly useful in designing peptides with specific structural or functional properties, such as those intended for biochemical studies or drug development. Additionally, the pyridyl moiety can enhance the solubility of peptides in aqueous solutions, making it valuable in creating biologically active compounds. Its application extends to research involving enzyme inhibitors, receptor ligands, and other bioactive molecules.
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...