4-tert-Butylcyclohexyl chloroformate

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Reagent Code: #141482
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CAS Number 42125-46-2

science Other reagents with same CAS 42125-46-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.72 g/mol
Formula C₁₁H₁₉ClO₂
inventory_2 Storage & Handling
Density 1.05 g/cm3 (20 °C)
Storage Room temperature, sealed

description Product Description

Used primarily as a reagent in organic synthesis, this compound serves as a protecting group agent for amines and alcohols due to its ability to form stable carbamates and carbonates. It is especially useful in peptide synthesis and pharmaceutical intermediates where selective protection is required. Its bulky tert-butyl group enhances steric hindrance, improving selectivity during reactions. Commonly employed in the preparation of protected amino acids and in multistep syntheses where mild deprotection conditions are needed. Also utilized in the development of agrochemicals and specialty polymers due to its reactivity and stability profile.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿49,150.00

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4-tert-Butylcyclohexyl chloroformate
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Used primarily as a reagent in organic synthesis, this compound serves as a protecting group agent for amines and alcohols due to its ability to form stable carbamates and carbonates. It is especially useful in peptide synthesis and pharmaceutical intermediates where selective protection is required. Its bulky tert-butyl group enhances steric hindrance, improving selectivity during reactions. Commonly employed in the preparation of protected amino acids and in multistep syntheses where mild deprotection

Used primarily as a reagent in organic synthesis, this compound serves as a protecting group agent for amines and alcohols due to its ability to form stable carbamates and carbonates. It is especially useful in peptide synthesis and pharmaceutical intermediates where selective protection is required. Its bulky tert-butyl group enhances steric hindrance, improving selectivity during reactions. Commonly employed in the preparation of protected amino acids and in multistep syntheses where mild deprotection conditions are needed. Also utilized in the development of agrochemicals and specialty polymers due to its reactivity and stability profile.

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