207990-68-9

Upstream product

• 108-98-5 thiophenol 
• 91597-65-8 [¹³C]methyl phenyl sulfide 

Downstream Products

• 92136-60-2 (13C)fluoromethyl phenyl sulfoxide 
• 1190788-60-3 (phenylthio) [13C]methyl 2,2,2-trifluoroacetate 
• 503533-74-2 [2H₃,13C]methyl phenyl sulfoxide 
• 1258075-02-3 methyl 4-(phenylsulfinyl)2-[3,4-13C₂]butenoate 
• 1258074-99-5 4-phenylsulfinyl-2[1,3,4-13C₃]butenoic acid 
• 1258074-89-3 4,4-diethoxy-1-(phenylsulfinyl)[1-13C]butan-2-one 
• 1258074-97-3 trans-4-(phenylsulfinyl)[4-13C]crotonic acid methyl ester 
• 207990-69-0 C₆⁽¹³⁾CH₇FO₂S 

Relevant academic research and scientific papers

Solute-solvent interactions and chiral induction in liquid crystals

The induction of a cholesteric phase by doping an achiral nematic liquid crystal with an enantiopure solute is a phenomenon that, as in all general supramolecular phenomena of chiral amplification, depends in a subtle way on intermolecular interactions. T

Stereoselective synthesis and X-ray structure determination of labeled [1, 2, 3-13C3]-1-(Phenylsulfinyl)-3-benzyloxyacetone

[1,2,3-13C3]-1-(Phenylsulfinyl)-3-benzyloxyacetone, C16H16O3S, (3) has been synthesized and its crystal structure has been determined by a single-crystal X-ray diffraction analysis. The X-ray diffract

Synthesis of isotopically labeled 1,3-dithiane

The 1,3-dithiane is a protected formaldehyde anion equivalent that could serve as a useful labeled synthon. We report a facile synthesis of 1,3-[2- 13C]- and 1,3-[2-13C, 2-2H2]dithiane in two steps from [13

SYNTHESIS OF PHOSPHONIC ACID LABELED COMPOUNDS

High purity isotopically labeled phosphonic acid esters can be obtained from isotopically enriched Chloro[13C]methyl phenyl sulfide The labeled phosphonic acid esters can then be used as precursors for the one step production of labeled vinyl sulfides, labeled vinyl sulfoxides, and labeled vinyl sulfones. The labeled phosphonic acid esters can also be reacted with a variety of aldehydes to produce extended vinyl systems that are isotopically labeled.