Dicyclohexylamine (S)-4-(((allyloxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)butanoate

≥95%

Reagent Code: #38489
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CAS Number 327156-92-3

science Other reagents with same CAS 327156-92-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 483.64 g/mol
Formula C₂₅H₄₅N₃O₆
badge Registry Numbers
MDL Number MFCD01862280
thermostat Physical Properties
Boiling Point 651.1°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the field of peptide chemistry. It serves as a key intermediate in the preparation of protected amino acid derivatives, which are essential for constructing peptides with specific sequences and functionalities. The compound’s structure, featuring both allyloxycarbonyl and tert-butoxycarbonyl protecting groups, allows for selective deprotection during multi-step synthetic processes. This selectivity is crucial in the development of pharmaceuticals, where precise control over molecular assembly is required. Additionally, its application extends to the production of bioactive compounds and research reagents, contributing to advancements in drug discovery and biochemical studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,782.00
inventory 5g
10-20 days ฿21,015.00
inventory 1g
10-20 days ฿6,732.00
inventory 250mg
10-20 days ฿2,736.00

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Dicyclohexylamine (S)-4-(((allyloxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)butanoate
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This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the field of peptide chemistry. It serves as a key intermediate in the preparation of protected amino acid derivatives, which are essential for constructing peptides with specific sequences and functionalities. The compound’s structure, featuring both allyloxycarbonyl and tert-butoxycarbonyl protecting groups, allows for selective deprotection during multi-step synthetic processes. This selectivity is cruci

This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the field of peptide chemistry. It serves as a key intermediate in the preparation of protected amino acid derivatives, which are essential for constructing peptides with specific sequences and functionalities. The compound’s structure, featuring both allyloxycarbonyl and tert-butoxycarbonyl protecting groups, allows for selective deprotection during multi-step synthetic processes. This selectivity is crucial in the development of pharmaceuticals, where precise control over molecular assembly is required. Additionally, its application extends to the production of bioactive compounds and research reagents, contributing to advancements in drug discovery and biochemical studies.

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