Tert-Butyl N-[4-(2-chloroacetamido)butyl]carbamate is a chemical compound characterized by its carbamate functional group, which is derived from the reaction of an amine with a carbonic acid derivative. This compound features a tert-butyl group, providing steric hindrance that can influence its reactivity and solubility. The presence of a chloroacetamido group suggests potential for reactivity in nucleophilic substitution reactions, making it useful in various synthetic applications. Its structure indicates that it may exhibit moderate polarity due to the presence of both hydrophobic (tert-butyl) and hydrophilic (carbamate and chloroacetamido) components. This dual nature can affect its solubility in different solvents, making it potentially soluble in organic solvents while having limited solubility in water. Additionally, the compound may exhibit biological activity, which could be of interest in pharmaceutical research. Safety data and handling precautions should be considered, as the chloroacetamido moiety may pose hazards typical of halogenated compounds. Overall, this compound's unique structure lends itself to various applications in organic synthesis and medicinal chemistry.

tert-Butyl N-[4-(2-chloroacetamido)butyl]carbamate

133264-58-1: Tert-Butyl N-[4-(2-chloroacetamido)butyl]carbamate is a chemical compound characterized by its carbamate functional group, which is derived from the reaction of an amine with a carbonic acid derivative. This compound features a tert-butyl group, providing steric hindrance that can influence its reactivity and solubility. The presence of a chloroacetamido group suggests potential for reactivity in nucleophilic substitution reactions, making it useful in various synthetic applications. Its structure indicates that it may exhibit moderate polarity due to the presence of both hydrophobic (tert-butyl) and hydrophilic (carbamate and chloroacetamido) components. This dual nature can affect its solubility in different solvents, making it potentially soluble in organic solvents while having limited solubility in water. Additionally, the compound may exhibit biological activity, which could be of interest in pharmaceutical research. Safety data and handling precautions should be considered, as the chloroacetamido moiety may pose hazards typical of halogenated compounds. Overall, this compound's unique structure lends itself to various applications in organic synthesis and medicinal chemistry.

tert-Butyl (4-(2-chloroacetamido)butyl)carbamate

<p>Chloroacetamido-C4-NHBoc is an alkyl/ether-based linker commonly employed in the synthesis of proteolysis targeting chimeras (PROTACs).</p>

CAS 133264-58-1

tert-Butyl N-[4-(2-chloroacetamido)butyl]carbamate

tert-Butyl (4-(2-chloroacetamido)butyl)carbamate

Ref: 54-OR1054146

Chloroacetamido-C4-NHBoc

Ref: TM-T38726