Sun, Tao et al. published their research in RSC Advances in 2019 | 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. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Application In Synthesis of Methyl heptanoate

Performance and selectivity of lower-rim substituted calix[4]arene as a stationary phase for capillary gas chromatography was written by Sun, Tao;Li, Bin;Shuai, Xiaomin;Chen, Yujie;Li, WeiWei;Cai, Zhiqiang;Qiao, Xiaoguang;Hu, Shaoqiang;Ma, Lufang. And the article was included in RSC Advances in 2019.Application In Synthesis of Methyl heptanoate The following contents are mentioned in the article:

This work presents the investigation of p-tert-butyl(tetradecyloxy)calix[4]arene (C4A-C10) as stationary phase for capillary gas chromatog. (GC) separations The statically-coated C4A-C10 capillary column showed weak polarity and column efficiency of 2566 plates per m determined by n-dodecane at 120°C. Impressively, the C4A-C10 column exhibited extremely high resolving capability for a wide range of analytes from nonpolar to polar, including n-alkanes, esters, ketones, aldehydes, alcs. and bromoalkanes. Most importantly, the C4A-C10 column exhibited an excellent separation performance for positional, structural and cis-/trans-isomers. Among them, the column displayed advantageous resolving capability over the com. polysiloxane stationary phase for aromatic amine isomers. Moreover, the C4A-C10 column showed good column repeatability with RSD values below 0.06% for run-to-run, 0.12-0.27% for day-to-day and 2.8-5.3% for column-to-column. 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. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Application In Synthesis of Methyl heptanoate

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