13084-34-9

Upstream product

• 13084-26-9 aziridine-1-carbothioic acid O-p-tolyl ester 
• 1483-41-6 1-bromo-2-isothiocyanatoethane 
• 1121-70-6 sodium 4-methylphenoxide 
• 937-63-3 p-Tolyl chlorothionoformate 
• 2576-47-8 2-bromoethylamine hydrobromide 

Downstream Products

• 91664-82-3 2-(S-(4-methylphenoxy)carbonylthio)ethyl isothiocyanates 
• 1187940-41-5 N-(4,5-dihydrothiazol-2-yl)-N-[3-(biphenyl-2-yl)-1-(2,3-dimethylphenyl)but-3-enyl]amine 
• 91664-90-3 N-(4-methoxyphenyl)-N'-2-(S-(4-methylphenoxy)carbonylthioethyl)thiourea 
• 91664-88-9 N-2-(S-(4-methylphenoxy)carbonylthioethyl)thiourea 

Relevant academic research and scientific papers

CHEMICAL COMPOUNDS

The use of a compound of formula (I) wherein X is (i), (ii) or (iii), formula (i),formula (ii), formula (iii) Y is O, S(O)m, NR3, CR5R6, CR5R6-CR7R8, O-CR7R

SYNTHESIS OF 2-(S-ARYLOXYCARBONYLTHIO)ETHYL ISOTHIOCYANATES - ANALOGUES OF NATURAL MUSTARD OILS

A simple reaction of 2-aryloxythiazolines with thiophosgene leads to formation of 2-(S-aryloxycarbonylthio)ethyl isothiocyanates.The starting thiazolines can easily be obtained from 2-bromoethyl isothiocyanates and phenolates.The structure of the products synthesized was evidenced by spectral methods.