D’Auria, Maurizio et al. published their research in Natural Product Research in 2021 | CAS: 5444-75-7

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Safety of 2-Ethylhexyl benzoate

The composition of the aroma of Serapias orchids in Basilicata (Southern Italy) was written by D’Auria, Maurizio;Lorenz, Richard;Mecca, Marisabel;Racioppi, Rocco;Romano, Vito Antonio. And the article was included in Natural Product Research in 2021.Safety of 2-Ethylhexyl benzoate The following contents are mentioned in the article:

The SPME-GC-MS anal. of the aroma components of Serapias cordigera, Serapias cordigera subsp. lucana, Serapias vomeracea, Serapias lingua, and Serapias parviflora were reported. The relevant components of the scent of Serapias cordigera were α-amorphene, Et oleate, heneicosane, heptadecane, 2-heptadecanone, Et elaidate, pentadecane, octadecane, farnesylacetaldehyde, nonadecane, and Et stearate. Serapias cordigera subsp. lucana gave α-amorphene, pentadecane, Pr undecanoate, heptadecane, Et elaidate and oleate, Et stearate, and 8-heptadecene. Serapias vomeracea showed pentadecane, 5-nonadecene, 1-nonadecene, 3-heptadecene, benzyl benzoate, 2-undecanone, and octadecane. Serapias lingua showed the presence of heptadecane, 3-heptadecene, iso-Pr myristate, pentadecane, nonadecane, iso-Pr palmitate, octadecane, and benzyl benzoate. Serapias parviflora gave pentadecane, pentadecene, hexadecane, heptadecane, nonadecane, and Et elaidate. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Safety of 2-Ethylhexyl benzoate).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Safety of 2-Ethylhexyl benzoate

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