112272-69-2

Basic information

• Product Name: C₉H₁₁N₂O₂⁽¹⁺⁾*I^(1-)
• CAS NO: 112272-69-2
• Molecular Weight: 306.103
• Mol File: 112272-69-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₉H₁₁N₂O₂⁽¹⁺⁾*I^(1-)(CAS DataBase Reference)
• NIST Chemistry Reference: C₉H₁₁N₂O₂⁽¹⁺⁾*I^(1-)(112272-69-2)
• EPA Substance Registry System: C₉H₁₁N₂O₂⁽¹⁺⁾*I^(1-)(112272-69-2)

Safety Data

• Hazardous Substances Data: 112272-69-2(Hazardous Substances Data)

Upstream product

• 94-63-3 pralidoxime iodide 
• 830-03-5 4-nitrophenol acetate 

Relevant articles and documents

Hydrolysis of carboxylate and phosphate esters using monopyridinium oximes in cationic micellar media

The reactions of p-nitrophenyl acetate (PNPA) with a series of monopyridinium oximes, viz. 2-PAM (2-hydroxyiminomethyl-1-methylpyridinium iodide), 3-PAM (3-hydroxyiminomethyl-1-methylpyridinium iodide), and 4-PAM (4-hydroxyiminomethyl-1-methylpyridinium iodide) have been studied in the presence of cationic surfactants of same hydrophobic chain length (C 16) within the concentration range of 0.5-6.0 mM at pH 8.0 under the pseudo-first-order condition. The observed rate constant (kobs) increases with increasing surfactant concentration culminating into a maximum, and this has been analyzed in detail following the concepts of micellar catalysis. The structure-activity relationship of the investigated oximes has been discussed, and 2-PAM was found to be the most reactive among all the three investigated oximes for the cleavage of PNPA. Esterolytic decomposition of p-nitrophenyldiphenyl phosphate with oximate ions (-CH=NO-) was followed in cetyltrimethylammonium bromide micelles at pH 9.0, and 4-PAM was the most reactive oxime for the micellar hydrolysis of phosphate ester. The apparent acid dissociation constants (pKa) of the investigated oximes have been determined spectrophotometrically.