Boc-L-α-Cyclohexylglycine

98%

Reagent Code: #104787
label
Alias BOC-L-cyclohexylglycine ; N-tert-butoxycarbonyl-L-cyclohexylglycine
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CAS Number 109183-71-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.33 g/mol
Formula C₁₃H₂₃NO₄
badge Registry Numbers
MDL Number MFCD00133638
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This chemical is primarily used in peptide synthesis as a building block for creating complex peptide structures. It serves as a protected amino acid derivative, where the Boc (tert-butoxycarbonyl) group safeguards the amino functionality during the synthesis process. This allows for selective deprotection and further modifications without disrupting the peptide chain. Its incorporation into peptides can enhance stability and influence the conformational properties of the final product. Additionally, it is utilized in pharmaceutical research for developing peptide-based drugs, particularly in targeting specific biological pathways or receptors. Its cyclohexyl side chain contributes to increased hydrophobicity, which can be beneficial in improving the pharmacokinetic properties of therapeutic peptides.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (T) 98
Specific Rotation [α]20/D (C = 1 in MeOH) 9-12
Appearance White To Light Yellow Powder
Infrared Spectrometry Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿2,760.00
inventory 1g
10-20 days ฿290.00
inventory 5g
10-20 days ฿630.00
Boc-L-α-Cyclohexylglycine
This chemical is primarily used in peptide synthesis as a building block for creating complex peptide structures. It serves as a protected amino acid derivative, where the Boc (tert-butoxycarbonyl) group safeguards the amino functionality during the synthesis process. This allows for selective deprotection and further modifications without disrupting the peptide chain. Its incorporation into peptides can enhance stability and influence the conformational properties of the final product. Additionally, it is utilized in pharmaceutical research for developing peptide-based drugs, particularly in targeting specific biological pathways or receptors. Its cyclohexyl side chain contributes to increased hydrophobicity, which can be beneficial in improving the pharmacokinetic properties of therapeutic peptides.
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