Boc-D-Serine methyl ester

98%

Reagent Code: #104700
label
Alias BOC-D-serine methyl ester
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CAS Number 95715-85-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.23 g/mol
Formula C₉H₁₇NO₅
badge Registry Numbers
MDL Number MFCD00270516
thermostat Physical Properties
Boiling Point 215 °C(lit.)
inventory_2 Storage & Handling
Density 1.08 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

This compound is primarily used in peptide synthesis as a building block. It serves as a protected form of D-serine, where the Boc (tert-butoxycarbonyl) group safeguards the amino functionality, and the methyl ester protects the carboxyl group. This dual protection allows selective reactions during peptide chain assembly, ensuring the desired sequence is achieved without unwanted side reactions. It is particularly valuable in the synthesis of complex peptides and proteins, especially those requiring D-serine incorporation for specific biological or structural properties. Additionally, it finds applications in pharmaceutical research for developing peptide-based drugs and in biochemical studies exploring peptide interactions and functions.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 98-100%
Specific Rotation [α]20/D (c=5, Methanol) 16-20
Appearance Colorless to yellow liquid or solid
Infrared Spectrometry Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,280.00
inventory 100g
10-20 days ฿4,900.00
inventory 5g
10-20 days ฿390.00
inventory 10g
10-20 days ฿720.00
Boc-D-Serine methyl ester
This compound is primarily used in peptide synthesis as a building block. It serves as a protected form of D-serine, where the Boc (tert-butoxycarbonyl) group safeguards the amino functionality, and the methyl ester protects the carboxyl group. This dual protection allows selective reactions during peptide chain assembly, ensuring the desired sequence is achieved without unwanted side reactions. It is particularly valuable in the synthesis of complex peptides and proteins, especially those requiring D-serine incorporation for specific biological or structural properties. Additionally, it finds applications in pharmaceutical research for developing peptide-based drugs and in biochemical studies exploring peptide interactions and functions.
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