Tert-butylcyclohexylcarbamate

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Reagent Code: #244605
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CAS Number 3712-40-1

science Other reagents with same CAS 3712-40-1

blur_circular Chemical Specifications

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Weight 199.29 g/mol
Formula C₁₁H₂₁NO₂
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MDL Number MFCD07127722
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It serves as a protecting group for amines during multi-step reactions due to the stability of the carbamate linkage under various reaction conditions. The tert-butyl group allows for selective deprotection under acidic conditions, making it valuable in peptide synthesis and the development of complex drug molecules. Its cyclohexyl structure adds conformational rigidity, which can influence the stereochemistry of reactions, aiding in the control of product selectivity. Also employed in the synthesis of agrochemicals and specialty polymers where controlled reactivity is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,120.00
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Tert-butylcyclohexylcarbamate
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It serves as a protecting group for amines during multi-step reactions due to the stability of the carbamate linkage under various reaction conditions. The tert-butyl group allows for selective deprotection under acidic conditions, making it valuable in peptide synthesis and the development of complex drug molecules. Its cyclohexyl structure adds conformational rigidity, which can influence the stereochemis

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It serves as a protecting group for amines during multi-step reactions due to the stability of the carbamate linkage under various reaction conditions. The tert-butyl group allows for selective deprotection under acidic conditions, making it valuable in peptide synthesis and the development of complex drug molecules. Its cyclohexyl structure adds conformational rigidity, which can influence the stereochemistry of reactions, aiding in the control of product selectivity. Also employed in the synthesis of agrochemicals and specialty polymers where controlled reactivity is required.

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