cis-ACOC is a bicyclic amino acid, which means that it contains a bicyclic structure that comprises of two rings. It has been widely used in the field of catalysis due to its unique stereochemistry. cis-ACOC is synthesized by the reaction of 1-aminocyclooctanol with acid anhydrides. The product obtained from this reaction is then subjected to further purification processes to obtain high purity cis-ACOC.
Applications of cis-ACOC
As mentioned earlier, cis-ACOC is widely used in the field of catalysis. Its unique stereochemistry makes it a potential candidate for the synthesis of biologically active compounds. It acts as a chiral auxiliary in several chemical reactions like Strecker synthesis, asymmetric aldol reaction, and Mannich reaction.
It is also used in the preparation of N-protected amino acids, which are widely used in peptide synthesis. cis-ACOC derivatives have also been used in the synthesis of β-lactams, which are essential components in the synthesis of antibiotics.
cis-ACOC in the Pharmaceutical Industry
cis-ACOC has gained importance in the pharmaceutical industry as it is used in the preparation of biologically active compounds. Its stereochemistry ensures that the synthesized compound is of high purity, which is essential for its activity.
In addition to the above-mentioned applications, cis-ACOC is also used in several other fields like analytical chemistry, material science, and protein engineering. Due to its multi-faceted applications, research on cis-ACOC has gained momentum in recent years.
CAS No: 69256-17-3
CAS No: 69256-17-3 is another important CAS number in the field of chemistry. It is the CAS number for N-Boc-cis-4-aminocyclohexanecarboxylic acid, which is a vital component used in peptide synthesis.
N-Boc-cis-4-aminocyclohexanecarboxylic acid is a derivative of cis-4-aminocyclohexanecarboxylic acid. It is synthesized by the reaction of 2-aminocyclohexanol with a Boc-anhydride. The product obtained from this reaction is then subjected to further purification processes to obtain high purity N-Boc-cis-4-aminocyclohexanecarboxylic acid.
In conclusion, cis-2-Amino-cyclooctanecarboxylic acid and its derivatives like N-Boc-cis-4-aminocyclohexanecarboxylic acid find multifaceted applications in chemistry and related fields. Their unique stereochemistry makes them suitable for the synthesis of biologically active compounds and has led to extensive research in recent years.