1-tert-Butoxycarbonyl-1,2,4-triazole

>97.0%(GC)

Reagent Code: #59052
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CAS Number 41864-24-8

science Other reagents with same CAS 41864-24-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.18 g/mol
Formula C₇H₁₁N₃O₂
badge Registry Numbers
MDL Number MFCD00042665
thermostat Physical Properties
Melting Point 47° C
Boiling Point 75 ° C /0.05kPa
inventory_2 Storage & Handling
Storage room temperature, inert gas

description Product Description

Widely used in organic synthesis as a protecting group for amines, particularly in peptide chemistry, to prevent unwanted reactions during complex molecule construction. It serves as an intermediate in the production of pharmaceuticals, enabling the development of active compounds by safeguarding reactive sites. Additionally, it is employed in the synthesis of agrochemicals and other specialty chemicals, where selective protection and deprotection of functional groups are critical. Its stability under various reaction conditions makes it a valuable tool in multi-step synthetic processes.

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inventory 5g
10-20 days ฿4,599.00

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1-tert-Butoxycarbonyl-1,2,4-triazole
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Widely used in organic synthesis as a protecting group for amines, particularly in peptide chemistry, to prevent unwanted reactions during complex molecule construction. It serves as an intermediate in the production of pharmaceuticals, enabling the development of active compounds by safeguarding reactive sites. Additionally, it is employed in the synthesis of agrochemicals and other specialty chemicals, where selective protection and deprotection of functional groups are critical. Its stability under va

Widely used in organic synthesis as a protecting group for amines, particularly in peptide chemistry, to prevent unwanted reactions during complex molecule construction. It serves as an intermediate in the production of pharmaceuticals, enabling the development of active compounds by safeguarding reactive sites. Additionally, it is employed in the synthesis of agrochemicals and other specialty chemicals, where selective protection and deprotection of functional groups are critical. Its stability under various reaction conditions makes it a valuable tool in multi-step synthetic processes.

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