13932-55-3

Basic information

• Product Name: Carbonic acid,esters,monophenyl ester
• CAS NO: 13932-55-3
• Molecular Weight: 138.123
• Mol File: 13932-55-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Carbonic acid,esters,monophenyl ester (CAS DataBase Reference)
• NIST Chemistry Reference: Carbonic acid,esters,monophenyl ester (13932-55-3)
• EPA Substance Registry System: Carbonic acid,esters,monophenyl ester (13932-55-3)

Safety Data

• Hazardous Substances Data: 13932-55-3(Hazardous Substances Data)

Upstream product

• 957188-25-9 4-methoxy-4'-methylbenzhydryl phenyl carbonate 
• 957188-24-8 4,4'-dimethylbenzhydryl phenyl carbonate 
• 31558-55-1 4-methoxybenzhydryl phenyl carbonate 
• 102-09-0 bis(phenyl) carbonate 
• 1268380-08-0 phenyl 4-formylphenyl carbonate 
• 1268380-09-1 phenyl 4-ethoxycarbonyl phenyl 
• 1268380-10-4 C₁₄H₁₀O₄ 
• 1268380-12-6 C₁₅H₁₂O₄ 
• 17175-11-0 phenyl O‐(4‐nitrophenyl) carbonate 
• 64897-41-2 3,4-dinitrophenyl phenyl carbonate 
• 476360-75-5 4-i[(phenoxycarbonyl)oxy]acetophenone 
• 1885-14-9 phenyl chloroformate 

Downstream Products

• 1245200-38-7 6-phenoxy-3-(pyridin-4-yl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazole 
• 1245200-52-5 2-phenoxy-5-(pyridin-4-yl)-1,3,4-oxadiazole 
• 39142-40-0 phenyl N-(2-thiazolyl)-carbamate 
• 1885-14-9 phenyl chloroformate 
• 93-99-2 benzoic acid phenyl ester 
• 1309654-01-0 6-chloro-N-(6-phenoxy-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-3-yl)benzo[d]thiazol-2-amine 
• 1309654-08-7 N-(6-chlorobenzo[d]thiazol-2-yl)-5-phenoxy-1,3,4-oxadiazol-2-amine 

Relevant articles and documents

Alkaline hydrolysis of Y-substituted phenyl phenyl thionocarbonates: Effect of changing electrophilic center from C=O to C=S on reactivity and mechanism

Second-order rate constants (kOH-) have been measured spectrophotometrically for reactions of Y-substituted phenyl phenyl thionocarbonates (4a-i) with OH- in 80 mol % H2O/20 mol % DMSO at 25.0 ± 0.1 °C. The ksu

Carbon kinetic isotope effects on the hydrolysis of aryl carbonates

Carbon kinetic isotope effects on the hydrolysis of aryl carbonates in 1:1 (v/v) dioxane-water at 25 °C at various pHs were used to calculate isotope effects on the reactions with hydroxide ion and with water. For diphenyl carbonate kOH12/kOH13 = 1.0482 and kw12/kw13 = 1.0509. For bis(p-methoxyphenyl)carbonate kOH12/kOH13= 1.0493 and kw12/kw13 = 1.0518. For bis(p-nitrophenyl)carbonate kOH12/KOH13 = 1.0476. The small change in the isotope effect with substituent group for both alkaline and neutral hydrolysis is in contrast to the large substituent effect on the rate constants for both reactions. The nearly constant isotope effect indicates that transition-state structures arc similar for all substrates.