389614-53-3

Basic information

• Product Name: PhI(ODNs)OH
• Synonyms: PhI(ODNs)OH;[Hydroxy-(2,4-dinitrobenzenesulfonyloxy)iodo] benzene
• CAS NO: 389614-53-3
• Molecular Formula: C₁₂H₉IN₂O₈S
• Molecular Weight: 468.17793
• Mol File: 389614-53-3.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: PhI(ODNs)OH(CAS DataBase Reference)
• NIST Chemistry Reference: PhI(ODNs)OH(389614-53-3)
• EPA Substance Registry System: PhI(ODNs)OH(389614-53-3)

Safety Data

• Hazardous Substances Data: 389614-53-3(Hazardous Substances Data)

Upstream product

• 591-50-4 iodobenzene 
• 89-02-1 2,4-dinitrobenzenesulfonic acid 
• 3240-34-4 [bis(acetoxy)iodo]benzene 

Downstream Products

• 518068-78-5 2,4-dinitro-benzenesulfonic acid 2-(4-chloro-phenyl)-1-methyl-2-oxo-ethyl ester 
• 518068-80-9 2,4-dinitro-benzenesulfonic acid 2-oxo-cyclohexyl ester 
• 1253201-07-8 2-(5-fluoropyridin-2-yl)-2-oxoethyl 2,4-dinitrobenzenesulfonate 
• 518068-82-1 C₁₇H₁₄N₂O₁₀S 

Relevant articles and documents

CALPAIN MODULATORS AND THERAPEUTIC USES THEREOF

Disclosed herein are small molecule calpain modulator compositions, pharmaceutical compositions, the use and preparation thereof.

Hypervalent iodine(iii) sulfonate mediated synthesis of quinoxalines in liquid peg-400

PEG-400[poly(ethylene glycol-400)] is used as a "green" recyclable solvent in the one-pot synthesis of quinoxalines by reaction with aryl ketones, hypervalent Iodine(III) Sulfonate, and o-phenylenediamines. Significant rate enhancements and improved yields have been observed.

Efficient Conversion of Alkyl Aryl Ketones to Aromatic Carboxylic Acids

An efficient method for the conversion of alkyl aryl ketones to aromatic carboxylic acids has been developed based on initial formation of α-organosulfonyloxy ketones and their subsequent oxidation reactions by tetrabutylammonium periodate in one-pot conditions.