tert-Butyl (3-methylbenzyl)carbamate

95%

Reagent Code: #82875
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CAS Number 179876-20-1

science Other reagents with same CAS 179876-20-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.30 g/mol
Formula C₁₃H₁₉NO₂
badge Registry Numbers
MDL Number MFCD21106051
thermostat Physical Properties
Boiling Point 337.9±21.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.020±0.06 g/cm3(Predicted)
Storage room temperature

description Product Description

This chemical is primarily used in organic synthesis as a protecting group for amines. It helps in preventing unwanted reactions of the amine group during complex chemical processes, particularly in the synthesis of pharmaceuticals and agrochemicals. Its stability under various reaction conditions makes it a valuable intermediate in the production of active pharmaceutical ingredients (APIs). Additionally, it can be employed in peptide synthesis to safeguard amino groups, ensuring selective reactions at other functional sites. Its use is also observed in the development of specialized polymers and resins, where controlled reactivity of amine groups is essential.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,512.00
inventory 1g
10-20 days ฿3,375.00
inventory 5g
10-20 days ฿6,750.00

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tert-Butyl (3-methylbenzyl)carbamate
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This chemical is primarily used in organic synthesis as a protecting group for amines. It helps in preventing unwanted reactions of the amine group during complex chemical processes, particularly in the synthesis of pharmaceuticals and agrochemicals. Its stability under various reaction conditions makes it a valuable intermediate in the production of active pharmaceutical ingredients (APIs). Additionally, it can be employed in peptide synthesis to safeguard amino groups, ensuring selective reactions at o

This chemical is primarily used in organic synthesis as a protecting group for amines. It helps in preventing unwanted reactions of the amine group during complex chemical processes, particularly in the synthesis of pharmaceuticals and agrochemicals. Its stability under various reaction conditions makes it a valuable intermediate in the production of active pharmaceutical ingredients (APIs). Additionally, it can be employed in peptide synthesis to safeguard amino groups, ensuring selective reactions at other functional sites. Its use is also observed in the development of specialized polymers and resins, where controlled reactivity of amine groups is essential.

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