BOC-N-METHYL-L-SERINE

95%

Reagent Code: #104825
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CAS Number 101772-29-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.23 g/mol
Formula C₉H₁₇NO₅
badge Registry Numbers
MDL Number MFCD00037249
thermostat Physical Properties
Melting Point 83-87°C
inventory_2 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.

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Test Parameter Specification
Appearance White Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,851.00
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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