Fmoc-D-Phg-OH

98%

Reagent Code: #66182
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CAS Number 111524-95-9

science Other reagents with same CAS 111524-95-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 373.4 g/mol
Formula C₂₃H₁₉NO₄
badge Registry Numbers
MDL Number MFCD00190891
thermostat Physical Properties
Melting Point 175-180°C
Boiling Point 606.3ºC at 760 mmHg
inventory_2 Storage & Handling
Density 1.299 g/cm3
Storage 2~8°C

description Product Description

Fmoc-D-Phg-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (9-fluorenylmethoxycarbonyl) group acts as a temporary protecting group for the amine functionality. This allows for the sequential addition of amino acids to build peptides with high precision. The D-configuration of phenylglycine (Phg) introduces chirality, which is crucial for creating peptides with specific stereochemical properties. This compound is especially valuable in the synthesis of bioactive peptides, peptidomimetics, and other complex molecules used in drug discovery and biochemical research. Its stability and compatibility with standard SPPS protocols make it a reliable choice for peptide chemists.

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Test Parameter Specification
Purity (HPLC) 98-100%
MP 175-180
Appearance White crystal

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿290.00
5g
10-20 days ฿680.00
25g
10-20 days ฿2,400.00
100g
10-20 days ฿8,250.00
Fmoc-D-Phg-OH
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Fmoc-D-Phg-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (9-fluorenylmethoxycarbonyl) group acts as a temporary protecting group for the amine functionality. This allows for the sequential addition of amino acids to build peptides with high precision. The D-configuration of phenylglycine (Phg) introduces chirality, which is crucial for creating peptides with specific stereochemical properties. T

Fmoc-D-Phg-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (9-fluorenylmethoxycarbonyl) group acts as a temporary protecting group for the amine functionality. This allows for the sequential addition of amino acids to build peptides with high precision. The D-configuration of phenylglycine (Phg) introduces chirality, which is crucial for creating peptides with specific stereochemical properties. This compound is especially valuable in the synthesis of bioactive peptides, peptidomimetics, and other complex molecules used in drug discovery and biochemical research. Its stability and compatibility with standard SPPS protocols make it a reliable choice for peptide chemists.

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