tert-butyl N-[(4-tert-butylphenyl)-cyanomethyl]carbamate

95%

Reagent Code: #87790
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CAS Number 774225-35-3

science Other reagents with same CAS 774225-35-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.39 g/mol
Formula C₁₇H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD24476515
inventory_2 Storage & Handling
Storage room temperature, dry, sealed

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile intermediate. It plays a crucial role in the preparation of complex molecules, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a tert-butyl group and a cyanomethyl moiety, makes it valuable for constructing nitrogen-containing compounds, such as amines and heterocycles. Additionally, it is employed in protecting group strategies during multi-step synthesis, where the carbamate group can be selectively removed or modified to achieve desired chemical transformations. Its application extends to research settings for exploring new chemical reactions and developing novel bioactive compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,059.00

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tert-butyl N-[(4-tert-butylphenyl)-cyanomethyl]carbamate
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This chemical is primarily utilized in organic synthesis as a versatile intermediate. It plays a crucial role in the preparation of complex molecules, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a tert-butyl group and a cyanomethyl moiety, makes it valuable for constructing nitrogen-containing compounds, such as amines and heterocycles. Additionally, it is employed in protecting group strategies during multi-step synthesis, where the carbamate group can

This chemical is primarily utilized in organic synthesis as a versatile intermediate. It plays a crucial role in the preparation of complex molecules, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a tert-butyl group and a cyanomethyl moiety, makes it valuable for constructing nitrogen-containing compounds, such as amines and heterocycles. Additionally, it is employed in protecting group strategies during multi-step synthesis, where the carbamate group can be selectively removed or modified to achieve desired chemical transformations. Its application extends to research settings for exploring new chemical reactions and developing novel bioactive compounds.

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