tert-Butyl 2-ethynylbenzylcarbamate

95%

Reagent Code: #146712
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CAS Number 1097731-47-9

science Other reagents with same CAS 1097731-47-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.29 g/mol
Formula C₁₄H₁₇NO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves as a protected amine building block in the construction of complex molecules, especially in the development of bioactive agents and drug candidates. The tert-butyl carbamate (Boc) group provides stability during reactions while allowing selective deprotection under mild acidic conditions. The ethynyl functionality enables further derivatization via click chemistry or coupling reactions, making it valuable in medicinal chemistry for creating libraries of compounds for biological screening. Commonly employed in the synthesis of protease inhibitors and receptor modulators.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,690.00
inventory 250mg
10-20 days ฿14,110.00

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tert-Butyl 2-ethynylbenzylcarbamate
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves as a protected amine building block in the construction of complex molecules, especially in the development of bioactive agents and drug candidates. The tert-butyl carbamate (Boc) group provides stability during reactions while allowing selective deprotection under mild acidic conditions. The ethynyl functionality enables further derivatization via click chemistry or coupling reactions,

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves as a protected amine building block in the construction of complex molecules, especially in the development of bioactive agents and drug candidates. The tert-butyl carbamate (Boc) group provides stability during reactions while allowing selective deprotection under mild acidic conditions. The ethynyl functionality enables further derivatization via click chemistry or coupling reactions, making it valuable in medicinal chemistry for creating libraries of compounds for biological screening. Commonly employed in the synthesis of protease inhibitors and receptor modulators.

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