1-(tert-Butyl)-4-(diethoxymethyl)-1H-1,2,3-triazole

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Reagent Code: #39570
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CAS Number 1257633-67-2

science Other reagents with same CAS 1257633-67-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.3033 g/mol
Formula C₁₁H₂₁N₃O₂
badge Registry Numbers
MDL Number MFCD25957226
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. Its structure, featuring a triazole ring and a diethoxymethyl group, makes it valuable in the development of pharmaceuticals and agrochemicals. The tert-butyl group enhances stability, allowing it to withstand harsh reaction conditions, while the diethoxymethyl moiety can act as a protecting group or be further functionalized. It is particularly useful in click chemistry reactions, where the triazole ring serves as a robust linker in drug discovery and material science applications. Additionally, it finds use in the preparation of polymers and coatings, where its unique properties contribute to improved performance and durability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,076.00

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1-(tert-Butyl)-4-(diethoxymethyl)-1H-1,2,3-triazole
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This chemical is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. Its structure, featuring a triazole ring and a diethoxymethyl group, makes it valuable in the development of pharmaceuticals and agrochemicals. The tert-butyl group enhances stability, allowing it to withstand harsh reaction conditions, while the diethoxymethyl moiety can act as a protecting group or be further functionalized. It is particularly useful in click chemistry reactions, whe

This chemical is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. Its structure, featuring a triazole ring and a diethoxymethyl group, makes it valuable in the development of pharmaceuticals and agrochemicals. The tert-butyl group enhances stability, allowing it to withstand harsh reaction conditions, while the diethoxymethyl moiety can act as a protecting group or be further functionalized. It is particularly useful in click chemistry reactions, where the triazole ring serves as a robust linker in drug discovery and material science applications. Additionally, it finds use in the preparation of polymers and coatings, where its unique properties contribute to improved performance and durability.

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