Reference

Isonitrosoacetophenone derivatives as phosphorylated cholinesterase reactivators

Isonitrosoacetophenone derivatives as phosphorylated cholinesterase reactivators. Structure-activity relationships. 92072-16-7 which is the cas registry number of some chemical is mentioned. Bonnafous, Monique; Bernadou, Jean; Fayet, Jean Pierre; Boudet-Dalbin, Raymond; Adam, Yves (Fac. Pharm., Univ. Paul Sabatier, Toulouse 31077, Fr.). Eur. J. Med. Chem. - Chim. Ther., 19(2), 123-30 (French) 1984. CODEN: EJMCA5. ISSN: 0009-4374. DOCUMENT TYPE: Journal CA Section: 4 (Toxicology) Section cross-reference(s): 22 Isonitrosoacetophenone (I; R = H) [532-54-7] and 12 derivs. (I; R = OH, Me, CF3, etc.) were studied in 2 ways with regard to their ability to reactivate organophosphate-inhibited cholinesterase [9001-08-5]: a kinetic model of reactivation and QSAR (Hansch model). The nucleophilic character of the oximate ion was of primary importance for the biol. activity. .

Determination of isonitrosoacetophenone using nonaqueous potentiometric titration

Determination of isonitrosoacetophenone using nonaqueous potentiometric titration. Khmel'nitskaya, E. Yu.; Selivanova, R. P.; Cherkasskii, A. A. (NII Org. Poluprod. Krasitelei, Moscow, USSR). Zavod. Lab., 50(1), 19-20 (Russian) 1984. CODEN: ZVDLAU. ISSN: 0044-1910. DOCUMENT TYPE: Journal CA Section: 80 (Organic Analytical Chemistry) The purity of isonitrosoacetophenone samples was detd. by a method involving extn. from solns. contg. KCl into CHCl3, diln. There are some commonly used reagents like 532-54-7 in this article. with DMSO, and potentiometric titrn. with 0.1 M KOH in alc. by using glass and Ag/AgCl electrodes. The relative error was within ±1.1%. .