BOC-N-METHYL-L-SERINE
95%
Reagent
Code: #104825
CAS Number
101772-29-6
blur_circular Chemical Specifications
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Molecular Information
Weight
219.23 g/mol
Formula
C₉H₁₇NO₅
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Registry Numbers
MDL Number
MFCD00037249
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Physical Properties
Melting Point
83-87°C
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Storage & Handling
Storage
Room temperature, sealed, dry
description Product Description
BOC-N-Methyl-L-Serine is widely used in peptide synthesis as a protecting group for amino acids. The BOC (tert-butoxycarbonyl) group safeguards the amine functionality during the synthesis process, ensuring selective reactions at other sites. This compound is particularly valuable in the preparation of complex peptides and proteins, where precise control over chemical reactions is essential. It is also employed in the development of pharmaceuticals, especially in the creation of peptide-based drugs, where it helps maintain the integrity of the peptide chain. Additionally, it finds applications in biochemical research for studying peptide structures and interactions. Its stability and ease of removal under mild acidic conditions make it a preferred choice in organic and medicinal chemistry.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | White Solid |
Purity (%) | 94.5-100 |
Infrared Spectrum | Conforms to Structure |
NMR | Conforms To Structure |
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BOC-N-METHYL-L-SERINE
BOC-N-Methyl-L-Serine is widely used in peptide synthesis as a protecting group for amino acids. The BOC (tert-butoxycarbonyl) group safeguards the amine functionality during the synthesis process, ensuring selective reactions at other sites. This compound is particularly valuable in the preparation of complex peptides and proteins, where precise control over chemical reactions is essential. It is also employed in the development of pharmaceuticals, especially in the creation of peptide-based drugs, where it helps maintain the integrity of the peptide chain. Additionally, it finds applications in biochemical research for studying peptide structures and interactions. Its stability and ease of removal under mild acidic conditions make it a preferred choice in organic and medicinal chemistry.
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