tert-Butyl hept-6-yn-1-ylcarbamate

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Reagent Code: #152734
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CAS Number 1192373-48-0

science Other reagents with same CAS 1192373-48-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.3 g/mol
Formula C₁₂H₂₁NO₂
badge Registry Numbers
MDL Number MFCD24467680
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a protected amine building block in organic synthesis, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions while allowing selective deprotection when needed. The terminal alkyne moiety enables further structural elaboration via click chemistry, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in the development of complex molecules, including bioactive compounds and functional materials. Its bifunctional nature supports use in conjugation strategies and the construction of molecular scaffolds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,770.00
inventory 250mg
10-20 days ฿2,980.00
inventory 1g
10-20 days ฿9,030.00
inventory 5g
10-20 days ฿29,340.00

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tert-Butyl hept-6-yn-1-ylcarbamate
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Used as a protected amine building block in organic synthesis, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions while allowing selective deprotection when needed. The terminal alkyne moiety enables further structural elaboration via click chemistry, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in the development of complex molecules, including bioactive compounds and funct

Used as a protected amine building block in organic synthesis, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions while allowing selective deprotection when needed. The terminal alkyne moiety enables further structural elaboration via click chemistry, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in the development of complex molecules, including bioactive compounds and functional materials. Its bifunctional nature supports use in conjugation strategies and the construction of molecular scaffolds.

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