tert-Butyl (1-cyclobutyl-2-oxoethyl)carbamate

95%

Reagent Code: #152889
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CAS Number 1781068-71-0

science Other reagents with same CAS 1781068-71-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.27 g/mol
Formula C₁₁H₁₉NO₃
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its structure allows for selective protection of amines, making it valuable in multi-step synthesis where controlled reactivity is needed. Commonly employed in the development of active pharmaceutical ingredients (APIs), especially in the preparation of beta-amino ketone derivatives. The tert-butyl carbamate group can be easily removed under mild acidic conditions, enabling efficient deprotection without damaging sensitive functional groups elsewhere in the molecule. Also utilized in the synthesis of agrochemicals and specialty polymers due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿9,500.00
inventory 100mg
10-20 days ฿13,670.00
inventory 250mg
10-20 days ฿22,770.00
inventory 1g
10-20 days ฿73,480.00

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tert-Butyl (1-cyclobutyl-2-oxoethyl)carbamate
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Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its structure allows for selective protection of amines, making it valuable in multi-step synthesis where controlled reactivity is needed. Commonly employed in the development of active pharmaceutical ingredients (APIs), especially in the preparation of beta-amino ketone derivatives. The tert-butyl carbamate group can be easily removed under mild acidic conditions, enabling effici

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its structure allows for selective protection of amines, making it valuable in multi-step synthesis where controlled reactivity is needed. Commonly employed in the development of active pharmaceutical ingredients (APIs), especially in the preparation of beta-amino ketone derivatives. The tert-butyl carbamate group can be easily removed under mild acidic conditions, enabling efficient deprotection without damaging sensitive functional groups elsewhere in the molecule. Also utilized in the synthesis of agrochemicals and specialty polymers due to its stability and reactivity profile.

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