155791-59-6

Basic information

• Product Name: Phosphoric acid 3-oxo-3H-1λ³-benzo[d][1,2]iodoxol-1-yl ester diphenyl ester
• Synonyms: Phosphoric acid 3-oxo-3H-1λ³-benzo[d][1,2]iodoxol-1-yl ester diphenyl ester
• CAS NO: 155791-59-6
• Molecular Weight: 496.195
• Mol File: 155791-59-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Phosphoric acid 3-oxo-3H-1λ³-benzo[d][1,2]iodoxol-1-yl ester diphenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphoric acid 3-oxo-3H-1λ³-benzo[d][1,2]iodoxol-1-yl ester diphenyl ester(155791-59-6)
• EPA Substance Registry System: Phosphoric acid 3-oxo-3H-1λ³-benzo[d][1,2]iodoxol-1-yl ester diphenyl ester(155791-59-6)

Safety Data

• Hazardous Substances Data: 155791-59-6(Hazardous Substances Data)

Upstream product

• 59457-26-0 1-chloro-1λ³-benzo[d][1,2]iodaoxol-3(1H)-one 
• 22350-95-4 silver(I) diphenylphosphonate 
• 10359-36-1 4-nitro-phenyl diphenyl phosphate 
• 304-91-6 o-iodosobenzoic acid 
• 84280-67-1 1-oxido-1,2-benziodoxol-3(1H)-one 

Downstream Products

• 838-85-7 diphenyl hydrogen phosphate 
• 131-62-4 1-hydroxy-1,2-benzodioxol-3-(1H)-one 
• 1829-23-8 1H,1'H-1,1'-oxy-bis-1λ³-benzo[d][1,2]iodoxol-3-one 
• 1829-26-1 1-acetoxy-1,2-benziodoxol-3-one 
• 142260-70-6 1-(tert-butylperoxy)-1,2-benziodoxol-3(1H)-one 
• 1829-25-0 1-methoxy-1λ³-benzo[d][1,2]iodaoxol-3(1H)-one 

Relevant articles and documents

A phosphorylated iodosobenzoate: The intermediate in the iodosobenzoate cleavage of a reactive phosphate

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A Quantitative Description of the Effect of Cetyltrimethylammonium Bromide on the 2-Iodosylbenzoate-Catalysed Hydrolysis of Active Esters and Related Compounds

Apparent second-order rate constants (k2(app)) for the reaction of 2-iodosylbenzoate with 4-nitrophenyl diphenyl phosphate (3), 4-nitrophenyl acetate (4), 1-methylethyl methyl-phosphonofluoridate (5), 1,2,2-trimethylpropyl methylphosphonofluoridate (6) and ethyl N,N-dimethylphosphoramidocyanidate (7) in solutions of cetyltrimethylammonium bromide (ctab) were determined over a range of ctab concentrations.The profiles of k2(app) against were analysed to obtain second-order rate constants for the reaction in the micellar phase, and stability constants for the binding of reactants to the micellized detergent.Reaction rates in the micellar and bulk aqueous phases for each substrate are indistinguishable.The rate enhancements provided by the micellized ctab result from concentrating the reactants in the micellar phase.Substrates (5)-(7) are much less strongly bound to the micellized detergent than (3), and the maximum rate enhancements for these substrates are correspondingly smaller.