Boc-N-methyl-L-valine dicyclohexylamine salt is a chemical compound that serves as a protected amino acid derivative, commonly used in peptide synthesis and pharmaceutical applications. The "Boc" (tert-butyloxycarbonyl) group is a protective group that shields the amino functionality during chemical reactions, allowing for selective modifications of other functional groups. The presence of the N-methyl group enhances the compound's lipophilicity and can influence its biological activity. The dicyclohexylamine component acts as a counterion, contributing to the solubility and stability of the salt form. This compound is typically characterized by its solid state at room temperature, and it may exhibit specific melting and solubility properties depending on the solvent used. Its applications often extend to the synthesis of more complex molecules in medicinal chemistry, where the protection and subsequent deprotection of functional groups are crucial for achieving desired structures. Safety data should be consulted for handling, as with all chemical substances, to ensure proper laboratory practices.

boc-N-methyl-L-valine dicyclohexylamine salt

35761-42-3: Boc-N-methyl-L-valine dicyclohexylamine salt is a chemical compound that serves as a protected amino acid derivative, commonly used in peptide synthesis and pharmaceutical applications. The "Boc" (tert-butyloxycarbonyl) group is a protective group that shields the amino functionality during chemical reactions, allowing for selective modifications of other functional groups. The presence of the N-methyl group enhances the compound's lipophilicity and can influence its biological activity. The dicyclohexylamine component acts as a counterion, contributing to the solubility and stability of the salt form. This compound is typically characterized by its solid state at room temperature, and it may exhibit specific melting and solubility properties depending on the solvent used. Its applications often extend to the synthesis of more complex molecules in medicinal chemistry, where the protection and subsequent deprotection of functional groups are crucial for achieving desired structures. Safety data should be consulted for handling, as with all chemical substances, to ensure proper laboratory practices.

CAS 35761-42-3

boc-N-methyl-L-valine dicyclohexylamine salt

BOC-MEVAL-OH DCHA

Ref: IN-DA00C7QF

Boc-N-Me-Val-OH dicyclohexylamine salt

Ref: 10-M03341