35948-66-4

Upstream product

• 95-57-8 2-monochlorophenol 
• 106-89-8 epichlorohydrin 

Downstream Products

• 1716-44-5 3-(2-Chlor-phenoxy)-2-hydroxy-propylfluorid 
• 85833-24-5 1-Butylsulfanyl-3-(2-chloro-phenoxy)-propan-2-ol 
• 95449-06-2 1-(2-Chloro-phenoxy)-3-hexylsulfanyl-propan-2-ol 
• 21925-70-2 3-<2-Chlor-phenoxy>-1-isopropylamino-propanol-(2) 
• 354527-90-5 1-(2-chloro-phenoxy)-3-pentylsulfanyl-propan-2-ol 
• 85833-36-9 o-Tolyl-carbamic acid 1-butylsulfanylmethyl-2-(2-chloro-phenoxy)-ethyl ester 
• 85833-42-7 Phenyl-thiocarbamic acid O-[1-butylsulfanylmethyl-2-(2-chloro-phenoxy)-ethyl] ester 
• 85833-30-3 Phenyl-carbamic acid 1-butylsulfanylmethyl-2-(2-chloro-phenoxy)-ethyl ester 
• 95449-24-4 m-Tolyl-carbamic acid 2-(2-chloro-phenoxy)-1-hexylsulfanylmethyl-ethyl ester 
• 95448-93-4 o-Tolyl-thiocarbamic acid O-[2-(2-chloro-phenoxy)-1-hexylsulfanylmethyl-ethyl] ester 
• 95449-18-6 o-Tolyl-carbamic acid 2-(2-chloro-phenoxy)-1-hexylsulfanylmethyl-ethyl ester 
• 95449-30-2 Phenyl-thiocarbamic acid O-[2-(2-chloro-phenoxy)-1-hexylsulfanylmethyl-ethyl] ester 
• 95449-12-0 Phenyl-carbamic acid 2-(2-chloro-phenoxy)-1-hexylsulfanylmethyl-ethyl ester 
• 946528-32-1 1-(2-chlorophenoxy)-3-thiocyanatopropan-2-one 

Relevant academic research and scientific papers

Asymmetric reduction of α-thiocyanatoketones by Saccharomyces cerevisiae and Mortierella isabellina-a new route to optically active thiiranes

A simple method for the preparation of optically active 1-aryloxy- and 1-arylsulphanyl-3-thiocyanatopropan-2-oles from racemic 1-chloro-3-aryloxy- and 1-chloro-3-arylsulphanyl-2-propanols via 1-aryloxy- and 1-arylsulphanyl-3-thiocyanatopropan-2-ones has been developed. The enantiomerically enriched β-hydroxythiocyanates were obtained by a microbiological reduction of the thiocyanatoketones with Saccharomyces cerevisiae or Mortierella isabellina and subsequently converted into optically active thiiranes on treatment with a lithium hydroxide solution.