(S)-tert-Butyl 6-amino-2-((tert-butoxycarbonyl)amino)hexanoate

98%

Reagent Code: #38587
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CAS Number 7750-42-7

science Other reagents with same CAS 7750-42-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.41 g/mol
Formula C₁₅H₃₀N₂O₄
badge Registry Numbers
MDL Number MFCD28963513
thermostat Physical Properties
Boiling Point 406.7±40.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. It serves as a key intermediate in the production of peptides, where the tert-butoxycarbonyl (Boc) group protects the amino group during the synthesis process, preventing unwanted reactions. The tert-butyl ester moiety also acts as a protective group for the carboxyl group, ensuring selective reactions at other sites. Its application is crucial in the development of pharmaceuticals, particularly in the synthesis of peptide-based drugs, where precise control over amino acid reactivity is essential. Additionally, it is used in research settings for studying peptide structures and functions, aiding in the design of novel therapeutic agents.

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Test Parameter Specification
Appearance Colorless to light yellow Viscous liquid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿13,662.00

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(S)-tert-Butyl 6-amino-2-((tert-butoxycarbonyl)amino)hexanoate
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This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. It serves as a key intermediate in the production of peptides, where the tert-butoxycarbonyl (Boc) group protects the amino group during the synthesis process, preventing unwanted reactions. The tert-butyl ester moiety also acts as a protective group for the carboxyl group, ensuring selective reactions at other sites. Its application is crucial in the development of pharmaceuticals, particularly in the synthesis of peptide-based drugs, where precise control over amino acid reactivity is essential. Additionally, it is used in research settings for studying peptide structures and functions, aiding in the design of novel therapeutic agents.
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