16-(tert-Butoxycarbonylamino)hexadecanoic acid, with the CAS number 135747-73-8, is a fatty acid derivative characterized by the presence of a long hydrocarbon chain and an amino group that is protected by a tert-butoxycarbonyl (Boc) group. This compound typically exhibits properties associated with both fatty acids and amines, including hydrophobic characteristics due to its long aliphatic chain, which contributes to its solubility in organic solvents. The Boc group serves as a protective group for the amino functionality, making it useful in synthetic organic chemistry, particularly in peptide synthesis and modifications. The presence of the carboxylic acid group allows for potential reactivity in various chemical reactions, such as esterification or amidation. Overall, this compound is significant in biochemical applications and research, particularly in the development of drug delivery systems and in the synthesis of bioactive molecules. Its stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in its handling and application.

16-(tert-butoxycarbonylamino)hexadecanoicacid

135747-73-8: 16-(tert-Butoxycarbonylamino)hexadecanoic acid, with the CAS number 135747-73-8, is a fatty acid derivative characterized by the presence of a long hydrocarbon chain and an amino group that is protected by a tert-butoxycarbonyl (Boc) group. This compound typically exhibits properties associated with both fatty acids and amines, including hydrophobic characteristics due to its long aliphatic chain, which contributes to its solubility in organic solvents. The Boc group serves as a protective group for the amino functionality, making it useful in synthetic organic chemistry, particularly in peptide synthesis and modifications. The presence of the carboxylic acid group allows for potential reactivity in various chemical reactions, such as esterification or amidation. Overall, this compound is significant in biochemical applications and research, particularly in the development of drug delivery systems and in the synthesis of bioactive molecules. Its stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in its handling and application.

16-((tert-Butoxycarbonyl)amino)hexadecanoic acid

CAS 135747-73-8

16-(tert-butoxycarbonylamino)hexadecanoicacid

16-((tert-Butoxycarbonyl)amino)hexadecanoic acid

Ref: 54-OR1069228

16-((tert-Butoxycarbonyl)amino)hexadecanoic acid

Ref: 10-F570651