tert-Butyl pent-4-yn-1-ylcarbamate

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Reagent Code: #122707
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CAS Number 151978-50-6

science Other reagents with same CAS 151978-50-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.25 g/mol
Formula C₁₀H₁₇NO₂
badge Registry Numbers
MDL Number MFCD20036287
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

description Product Description

This chemical is primarily used in organic synthesis as a protective group for amines. The tert-butyl group provides stability under various reaction conditions, allowing selective modification of other functional groups in the molecule. It is particularly useful in peptide synthesis, where it protects the amine group during the formation of peptide bonds. Additionally, the pent-4-yn-1-yl moiety can participate in click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition, enabling the attachment of diverse functional groups or biomolecules. This makes it valuable in the development of pharmaceuticals, bioconjugation, and materials science for creating complex molecular architectures.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,260.00
inventory 5g
10-20 days ฿8,838.00
inventory 1g
10-20 days ฿2,727.00

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tert-Butyl pent-4-yn-1-ylcarbamate
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This chemical is primarily used in organic synthesis as a protective group for amines. The tert-butyl group provides stability under various reaction conditions, allowing selective modification of other functional groups in the molecule. It is particularly useful in peptide synthesis, where it protects the amine group during the formation of peptide bonds. Additionally, the pent-4-yn-1-yl moiety can participate in click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition, enablin

This chemical is primarily used in organic synthesis as a protective group for amines. The tert-butyl group provides stability under various reaction conditions, allowing selective modification of other functional groups in the molecule. It is particularly useful in peptide synthesis, where it protects the amine group during the formation of peptide bonds. Additionally, the pent-4-yn-1-yl moiety can participate in click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition, enabling the attachment of diverse functional groups or biomolecules. This makes it valuable in the development of pharmaceuticals, bioconjugation, and materials science for creating complex molecular architectures.

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