H-Cha-OH

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Reagent Code: #194701
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CAS Number 27527-05-5

science Other reagents with same CAS 27527-05-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.24 g/mol
Formula C₉H₁₇NO₂
badge Registry Numbers
MDL Number MFCD00153484
thermostat Physical Properties
Melting Point 322°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

H-Cha-OH, also known as Cyclohexylalanine, is a non-proteinogenic amino acid widely used in peptide synthesis to incorporate a hydrophobic, bulky side chain that enhances peptide stability against enzymatic degradation and improves pharmacokinetic properties such as bioavailability and membrane permeability. It serves as a phenylalanine analog, enabling the design of bioactive peptides, enzyme inhibitors, and peptidomimetics with reduced immunogenicity and increased metabolic stability. Compatible with standard coupling reagents, it is employed in both solution-phase and solid-phase synthesis for pharmaceutical research and development.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿174.00
inventory 5g
10-20 days ฿450.00
inventory 25g
10-20 days ฿1,700.00
inventory 100g
10-20 days ฿6,700.00

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H-Cha-OH
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H-Cha-OH, also known as Cyclohexylalanine, is a non-proteinogenic amino acid widely used in peptide synthesis to incorporate a hydrophobic, bulky side chain that enhances peptide stability against enzymatic degradation and improves pharmacokinetic properties such as bioavailability and membrane permeability. It serves as a phenylalanine analog, enabling the design of bioactive peptides, enzyme inhibitors, and peptidomimetics with reduced immunogenicity and increased metabolic stability. Compatible with s

H-Cha-OH, also known as Cyclohexylalanine, is a non-proteinogenic amino acid widely used in peptide synthesis to incorporate a hydrophobic, bulky side chain that enhances peptide stability against enzymatic degradation and improves pharmacokinetic properties such as bioavailability and membrane permeability. It serves as a phenylalanine analog, enabling the design of bioactive peptides, enzyme inhibitors, and peptidomimetics with reduced immunogenicity and increased metabolic stability. Compatible with standard coupling reagents, it is employed in both solution-phase and solid-phase synthesis for pharmaceutical research and development.

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