Boc-D-Phg-OH

98%

Reagent Code: #104725
label
Alias BOC-D-phenylglycine ; N-tert-butoxycarbonyl-D-phenylglycine
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CAS Number 33125-05-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.28 g/mol
Formula C₁₃H₁₇NO₄
badge Registry Numbers
MDL Number MFCD00062043
thermostat Physical Properties
Melting Point 88-91 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used extensively in peptide synthesis as a protective group for amino acids, ensuring selective reactions during the formation of peptide bonds. It is particularly valuable in the preparation of complex peptides and proteins, where precise control over the sequence and structure is crucial. Additionally, it finds application in the development of pharmaceuticals, aiding in the creation of peptide-based drugs with enhanced stability and bioavailability. Its role in organic synthesis also extends to the production of chiral compounds, contributing to the synthesis of enantiomerically pure substances for various industrial and research purposes.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White To Almost White Powder To Crystal
Purity (%) 97.5-100%
Melting Point (°C) 89.0-93.0
Infrared Spectrum Conforms To Structure
Specific Rotation [a]20/D (C=1, EtOH) -135.0 to -145.0

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days Ft3,581.72
inventory 1g
10-20 days Ft2,967.71
inventory 25g
10-20 days Ft7,368.11
inventory 100g
10-20 days Ft20,262.30
Boc-D-Phg-OH
Used extensively in peptide synthesis as a protective group for amino acids, ensuring selective reactions during the formation of peptide bonds. It is particularly valuable in the preparation of complex peptides and proteins, where precise control over the sequence and structure is crucial. Additionally, it finds application in the development of pharmaceuticals, aiding in the creation of peptide-based drugs with enhanced stability and bioavailability. Its role in organic synthesis also extends to the production of chiral compounds, contributing to the synthesis of enantiomerically pure substances for various industrial and research purposes.
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