Boc-D-Glu(ochex)-OH

97%

Reagent Code: #104696
label
Alias BOC-D-GLUTAMIC ACID(OCHEX)-OH;N-[(1,1-Dimethylethoxy)Carbonyl]-D-Glutamic Acid 5-Cyclohexyl Ester;BOC-D-GLUTAMIC ACID Y-CYCLOHEXYLESTER
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CAS Number 133464-27-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 329.40 g/mol
Formula C₁₆H₂₇NO₆
badge Registry Numbers
MDL Number MFCD00076929
thermostat Physical Properties
Boiling Point 502.6±45.0 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.2±0.1 g/cm3
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily used in peptide synthesis as a protected form of glutamic acid. The Boc (tert-butoxycarbonyl) group serves as a protective group for the amino functionality, while the OChex (cyclohexyl ester) group protects the carboxylic acid side chain of glutamic acid. This protection is crucial during the stepwise assembly of peptides to prevent unwanted side reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection and coupling steps are required to build the peptide chain. The compound ensures the precise incorporation of glutamic acid into the desired peptide sequence, making it essential in the development of pharmaceuticals, bioactive peptides, and research applications involving peptide-based studies.

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Test Parameter Specification
Appearance Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,890.00
Boc-D-Glu(ochex)-OH
This compound is primarily used in peptide synthesis as a protected form of glutamic acid. The Boc (tert-butoxycarbonyl) group serves as a protective group for the amino functionality, while the OChex (cyclohexyl ester) group protects the carboxylic acid side chain of glutamic acid. This protection is crucial during the stepwise assembly of peptides to prevent unwanted side reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection and coupling steps are required to build the peptide chain. The compound ensures the precise incorporation of glutamic acid into the desired peptide sequence, making it essential in the development of pharmaceuticals, bioactive peptides, and research applications involving peptide-based studies.
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