Fernandez Montoya, Deicy J. et al. published their research in Natural Product Research in 2021 | CAS: 106-73-0

Methyl heptanoate (cas: 106-73-0) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Application In Synthesis of Methyl heptanoate

Enantiomeric synthesis of natural alkylglycerols and their antibacterial and antibiofilm activities was written by Fernandez Montoya, Deicy J.;Contreras Jordan, Luis A.;Moreno-Murillo, Barbara;Silva-Gomez, Edelberto;Mayorga-Wandurraga, Humberto. And the article was included in Natural Product Research in 2021.Application In Synthesis of Methyl heptanoate The following contents are mentioned in the article:

Alkylglycerols (AKGs) are bioactive natural compounds that vary by alkyl chain length and degree of unsaturation, and their absolute configuration is 2S. Three AKGs were synthesized in enantiomerically pure form, and were characterized for the 1st time together with 12 other known and naturally occurring AKGs. Their structures were established using 1H and 13C APT NMR with 2D-NMR, ESI-MS, or HRESI-MS and optical rotation data, and they were tested for their antibacterial and antibiofilm activities. Some AKGs showed activity against 5 clin. isolates and Pseudomonas aeruginosa ATCC 15442, with MIC values in the range of 15-125μg/mL. In addition, at half of the MIC, most of the AKGs reduced Staphylococcus aureus biofilm formation in the range of 23-99% and P. aeruginosa ATCC 15442 biofilm formation in the range of 14-64%. The antibiofilm activity of the AKGs assessed in this work had not previously been studied. This study involved multiple reactions and reactants, such as Methyl heptanoate (cas: 106-73-0Application In Synthesis of Methyl heptanoate).

Methyl heptanoate (cas: 106-73-0) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Application In Synthesis of Methyl heptanoate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics