N-Carbobenzoxy-D-2-phenylglycine

≥99%

Reagent Code: #76566
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CAS Number 17609-52-8

science Other reagents with same CAS 17609-52-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.30 g/mol
Formula C₁₆H₁₅NO₄
badge Registry Numbers
MDL Number MFCD00021703
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

N-Carbobenzoxy-D-2-phenylglycine is primarily used in peptide synthesis as a protecting group for amino acids. It helps in the selective protection of the amino group during the formation of peptide bonds, ensuring that the desired sequence is achieved without unwanted side reactions. This compound is particularly valuable in the synthesis of complex peptides and proteins, where precise control over the reaction process is crucial. Additionally, it finds application in the preparation of chiral intermediates for pharmaceuticals, contributing to the development of enantiomerically pure drugs. Its role in organic synthesis extends to the creation of biologically active molecules, making it a key reagent in medicinal chemistry and biochemical research.

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Test Parameter Specification
Purity 99-100%
Appearance White to Off-White Crystals Powder

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿550.00
5g
10-20 days ฿2,490.00
25g
10-20 days ฿6,640.00
100g
10-20 days ฿17,928.00
N-Carbobenzoxy-D-2-phenylglycine
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N-Carbobenzoxy-D-2-phenylglycine is primarily used in peptide synthesis as a protecting group for amino acids. It helps in the selective protection of the amino group during the formation of peptide bonds, ensuring that the desired sequence is achieved without unwanted side reactions. This compound is particularly valuable in the synthesis of complex peptides and proteins, where precise control over the reaction process is crucial. Additionally, it finds application in the preparation of chiral intermediates for pharmaceuticals, contributing to the development of enantiomerically pure drugs. Its role in organic synthesis extends to the creation of biologically active molecules, making it a key reagent in medicinal chemistry and biochemical research.
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