Boc-L-α-Cyclohexylglycine
98%
Reagent
Code: #104787
Alias
BOC-L-cyclohexylglycine ; N-tert-butoxycarbonyl-L-cyclohexylglycine
CAS Number
109183-71-3
blur_circular Chemical Specifications
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Molecular Information
Weight
257.33 g/mol
Formula
C₁₃H₂₃NO₄
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Registry Numbers
MDL Number
MFCD00133638
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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 |
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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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