Methoxy(phenylthio)methane as an ambi-equivalent of a methoxy- or (phenylthio)methylene 1,1-dipole was written by Sato, Tsuneo;Okura, Shuji;Otera, Junzo;Nozaki, Hitoshi. And the article was included in Tetrahedron Letters in 1987.HPLC of Formula: 50767-78-7 The following contents are mentioned in the article:
MeOCHRSPh [R = (CH2)8H, (CH2)8OSiMe2CMe3, CH2CH:CMe2, Ph], prepared by alkylation of MeOCH2SPh, are allylated by R1CR2:CHR3CH2SnBu3 (R1-R3 = H; R1 = R2 = H, R3 = Me; R1 = R2 = Me, R3 = H; R1 = Me, R2 = R3 = H) in the presence of BF3·OEt2 to give almost entirely MeOCHRCR1R2CR3:CH2. In the presence of TiCl4, however, the product is almost entirely PhSCHRCR1R2CR3:CH2. This study involved multiple reactions and reactants, such as (E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7HPLC of Formula: 50767-78-7).
(E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. 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.HPLC of Formula: 50767-78-7
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics