118712-54-2

Basic information

• Product Name: glycidyl p-toluenesulfonate
• Synonyms: glycidyl p-toluenesulfonate
• CAS NO: 118712-54-2
• Molecular Weight: 228.269
• Mol File: 118712-54-2.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: glycidyl p-toluenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: glycidyl p-toluenesulfonate(118712-54-2)
• EPA Substance Registry System: glycidyl p-toluenesulfonate(118712-54-2)

Safety Data

• Hazardous Substances Data: 118712-54-2(Hazardous Substances Data)

Upstream product

• 556-52-5 oxiranyl-methanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 96-24-2 3-monochloro-1,2-propanediol 
• 104-15-4 toluene-4-sulfonic acid 
• 4873-09-0 allyl tosylate 

Downstream Products

• 152467-59-9 Toluene-4-sulfonic acid 3-(6-chloro-hexyloxy)-2-hydroxy-propyl ester 
• 144912-01-6 Diethyl 3-hydroxy-4-(p-toluenesulfonyloxy)butanephosphonate 
• 2461-42-9 3-(1-naphthyloxy)-1,2-epoxypropane 
• 145939-36-2 2-hydroxy-6-(trimethylsilyl)-4-hexynyl tosylate 
• 81147-94-6 methyl 3-<4-(2,3-epoxypropoxy)phenyl>propionate 
• 118629-71-3 Toluene-4-sulfonic acid (S)-3-cyclohexyl-2-hydroxy-propyl ester 
• 2930-05-4 Benzyloxymethyl-oxiran 
• 138806-50-5 2-hydroxy-4-phenylthio-6-trimethylsilyl-5-hexynyl tosylate 
• 133242-64-5 (2,2-dimethyl-1,3-dioxolan4-yl)methyl 3-[4-(2,3-epoxypropoxy)-phenyl]propionate 
• 125830-44-6 Toluene-4-sulfonic acid (E)-3-hydroxy-propenyl ester 
• 142545-51-5 3-fluoro-1,2-propanediol 1-O-(4-methylbenzene)sulphonate 
• 168431-73-0 1-azido-3-(p-toluenesulfonyloxy)propan-2-ol 
• 40879-42-3 2-hydroxypropane-1,3-diyl bis(4-methylbenzenesulfonate) 
• 828-25-1 (+/-)-3-(4-iodophenoxy)-1,2-epoxypropane 

Relevant articles and documents

Glycidyl Tosylate: Polymerization of a “Non-Polymerizable” Monomer permits Universal Post-Functionalization of Polyethers

Glycidyl tosylate appears to be a non-polymerizable epoxide when nucleophilic initiators are used because of the excellent leaving group properties of the tosylate. However, using the monomer-activated mechanism, this unusual monomer can be copolymerized

Synthesis and characterization of new 3-(4-arylpiperazin-1-yl)-2-hydroxypropyl 4-propoxybenzoates and their hydrochloride salts

Five new 3-(4-arylpiperazin-1-yl)-2-hydroxypropyl 4-propoxybenzoates were designed and synthesized as potential dual antihypertensive agents. The compounds were prepared as free bases and subsequently transformed to hydrochloride salts. The position of pr

Dihydroquinozinone carboxylic acid compound and application thereof (by machine translation)

The invention belongs to the field of, pharmaceutical chemistry, and relates to (HBV) a dihydroquinozinone carboxylic acid compound with the activity of, and resisting hepatitis B virus (hepatitis B virus) .and a preparation method of the dihydroquinozino

Synthesis and determination of physicochemical properties of new 3-(4-arylpiperazin-1-yl)-2-hydroxypropyl 4-alkoxyethoxybenzoates

Nine new dihydrochloride salts of 3-(4-arylpiperazin-1-yl)-2-hydroxypropyl 4-alkoxyethoxybenzoates were designed and synthesized. The physicochemical properties such as lipophilicity index (log kw) and dissociation constant (pKa) wer