(R)-2-(((Benzyloxy)carbonyl)(methyl)amino)-4-methylpentanoic acid

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Reagent Code: #37438
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CAS Number 65635-85-0

science Other reagents with same CAS 65635-85-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.33 g/mol
Formula C₁₅H₂₁NO₄
thermostat Physical Properties
Boiling Point 419.4±34.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily used in the synthesis of peptides and peptidomimetics, serving as a key intermediate in the development of pharmaceutical agents. It is particularly valuable in the preparation of modified amino acids, which are crucial for creating peptide-based drugs with enhanced stability and bioavailability. The benzyloxycarbonyl (Cbz) protecting group in the molecule allows for selective deprotection during peptide synthesis, enabling precise control over the assembly of complex peptide structures. Additionally, its chiral center makes it useful in the production of enantiomerically pure compounds, which are essential for drugs targeting specific biological pathways with minimal side effects.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿3,681.00
inventory 1g
10-20 days ฿1,062.00
inventory 250mg
10-20 days ฿531.00

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(R)-2-(((Benzyloxy)carbonyl)(methyl)amino)-4-methylpentanoic acid
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This compound is primarily used in the synthesis of peptides and peptidomimetics, serving as a key intermediate in the development of pharmaceutical agents. It is particularly valuable in the preparation of modified amino acids, which are crucial for creating peptide-based drugs with enhanced stability and bioavailability. The benzyloxycarbonyl (Cbz) protecting group in the molecule allows for selective deprotection during peptide synthesis, enabling precise control over the assembly of complex peptide s

This compound is primarily used in the synthesis of peptides and peptidomimetics, serving as a key intermediate in the development of pharmaceutical agents. It is particularly valuable in the preparation of modified amino acids, which are crucial for creating peptide-based drugs with enhanced stability and bioavailability. The benzyloxycarbonyl (Cbz) protecting group in the molecule allows for selective deprotection during peptide synthesis, enabling precise control over the assembly of complex peptide structures. Additionally, its chiral center makes it useful in the production of enantiomerically pure compounds, which are essential for drugs targeting specific biological pathways with minimal side effects.

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