Detail of "1126-00-7"

Reference

Stable liquid pyrazole derivative insecticidal formulations

Stable liquid pyrazole derivative insecticidal formulations. Gautier, Martine; Derois, Jean (Rhone-Poulenc Agrochimie; Gautier, Martine; Derois, Jean, Fr.). PCT Int. Appl. WO 9701278 A1 16 Jan 1997, 22 pp. DESIGNATED STATES: W: AL, AU, BB, BG, BR, CA, CN, CZ, EE, GE, HU, IL, IS, JP, KP, KR, LK, LR, LT, LV, MG, MK, MN, MX, NO, NZ, PL, RO, SG, SI, SK, TR, TT, UA, US, UZ, VN, AM, AZ, BY, KG, KZ, MD, RU, TJ, TM; RW: AT, BE, BF, BJ, CF, CG, CH, CI, CM, DE, DK, ES, FI, FR, GA, GB, GR, IE, IT, LU, MC, ML, MR, NE, NL, PT, SE, SN, TD, TG. (French). (World Intellectual Property Organization). CODEN: PIXXD2. CLASS: ICM: A01N047-02. ICS: A01N043-56. ICI: A01N047-02, A01N025-00; A01N043-56, A01N025-00. APPLICATION: WO 1996-FR993 26 Jun 1996. PRIORITY: FR 1995-8073 29 Jun 1995; US 1995-7747 13 Oct 1995. DOCUMENT TYPE: Patent CA Section: 5 (Agrochemical Bioregulators) Insecticidal compns. include: 0.001-5 %, preferably 0.05-0.5 % 1-phenylpyrazole deriv. insecticide (Markush given), particularly fipronil, 0.05-10 %, preferably 0.1-5 % thickening agent, and 5-50 %, preferably 10-40 % propylene glycol. The pyrazole deriv.In this experiment, several chemicals are used like 1126-00-7 and 57-55-6 is dissolved in propylene glycol. An insect control method using the compn., particularly for controlling ants, is also disclosed. .

Preparation and characterization of carbene complexes of iron from azolyl and thienyl precursors

Preparation and characterization of carbene complexes of iron from azolyl and thienyl precursors. Raubenheimer, Helgard G.; Desmet, Mieke; Olivier, Pierre; Kruger, Gert J. (Department Chemistry Biochemistry, Rand Afrikaans University, Auckland Park 2006, S. Afr.). Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry, (23), 4431-4438 (English) 1996 Royal Society of Chemistry. CODEN: JCDTBI. ISSN: 0300-9246. DOCUMENT TYPE: Journal CA Section: 29 (Organometallic and Organometalloidal Compounds) Section cross-reference(s): 75 Azolyl and thienyl Fe(II) complexes were synthesized by the addn. of 1-phenylpyrazol-5-yllithium, 5-(4,5-dihydro-4,4-dimethyloxazolin-2-yl)-2-thienyllithium, 2-(4,5-dihydro-4,4-dimethyloxazolin-2-yl)-3-thienyllithium or 5-(2-pyridyl)-2-thienyllithium to [Fe(Cp)(CO)2Cl] (Cp = h-C5H5). Protonation or alkylation of these precursor complexes yielded the corresponding amino(organo)-, organo(thio)- or heterometallacyclic alkoxy(amino)- and hydroxy(amino)carbene complexes as well as compds. in which the ligand shows more pyridinium character. The mol. structures of the pyrazolyl complex [Fe(Cp)(CO)2(C:CHCH:NNPh)] I and the pyrazolinylidene complex [Fe(Cp)(CO)2(CCH:CHNHNPh)][CF3SO3] II have Fe-C bond lengths of 1.98(2) and 1. 1126-00-7 is just another one chemical used in this study.969(5) ? resp. .