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Detail of "75867-00-4"

  • CAS Number:
  • 75867-00-4
  • Name:
  • Cyclopropanecarboxylicacid, 3-(2,2-dichloroethenyl)-2,2-dimethyl-,(2,3,4,5,6-pentafluorophenyl)methyl ester, (1R,3S)-

  • Molecular Structure:
  • Formula:
  • C15H11 Cl2 F5 O2
  • Molecular Weight:
  • 389.16
  • Synonyms:
  • Cyclopropanecarboxylicacid, 3-(2,2-dichloroethenyl)-2,2-dimethyl-, (pentafluorophenyl)methyl ester,(1R,3S)- (9CI); Cyclopropanecarboxylic acid,3-(2,2-dichloroethenyl)-2,2-dimethyl-, (pentafluorophenyl)methyl ester,(1R-trans)-; Fenfluthrin; NAK 1654
  • Safety:
  • Moderately toxic by intravenous route. When heated to decomposition it emits toxic vapors of F and Cl. Details

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CAS No.75867-00-4 Cyclopropanecarboxylicacid, 3-(2,2-dichloroethenyl)-2,2-dimethyl-,(2,3,4,5,6-pentafluorophenyl)methyl ester, (1R,3S)-

Assay:98%

Supplier:Hangzhou Dayangchem Co., Ltd. [ China (Mainland)]

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CAS No.75867-00-4 Cyclopropanecarboxylicacid, 3-(2,2-dichloroethenyl)-2,2-dimethyl-,(2,3,4,5,6-pentafluorophenyl)methyl ester, (1R,3S)-

Supplier:China Surchem International [ China (Mainland)]

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Address:A23006 Jinma Square, No. 39 North Huaihai Rd, Huai An 223001, Jiangsu, China

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Reference

Properties and potentialities of NAK 1654 (fenfluthrin), a new pyrethroid for the control of household, public health and stored-product pests
Properties and potentialities of NAK 1654 (fenfluthrin), a new pyrethroid for the control of household, public health and stored-product pests. Behrenz, W.; Naumann, K. (Biol. Forsch., Bayer AG, Leverkusen, Fed. Rep. Ger.). Pflanzenschutz-Nachr., 35(3), 309-49 (English) 1982. CODEN: PFZNAQ. ISSN: 0079-1342. DOCUMENT TYPE: Journal CA Section: 5 (Agrochemical Bioregulators) The chem., properties, toxicol., formulations, and biol. effects of NAK 1654 (I) [75867-00-4] are reported. The knockdown effect of I against Musca domestica, Fannia canicularis, Stomoxys calcitrans, Calliphora erythrocephala, Lucilia sericata, Chrysomya putoria, Aedes aegypti, Anopheles stephensi, Xenopsylla cheopis, Blattella germanica, Blatta orientalis, Periplaneta americana, Acheta domesticus, Cimex lectularis, Rhodinus prolixus, Triatoma infestans, Lasius niger, Niptus holoeucus, Gibbium psylloides, Anthrenus fasciatus, Attagenus piceus, Dermestes peruvianus, Sitophilus granarius, Tribolium confusum, Rhizopertha dominica, Tenebroides mauritanicus, and Ornithodoros moubata were compared with those of other insecticides, e.g., deltamethrin, permethrin, and propoxur. The LD50 values of I in housefly showed its superiority to other insecticides, e.g., tetramethrin, bioallethrin, bioresmethrin, pyrethrins, propoxur, bendiocarb, and dichlorvos. Aerosol and smoke formulations of I against mosquitoes and housefly are discussed.
Synergist for pyrethroid insecticides
Synergist for pyrethroid insecticides. Behrenz, Wolfgang; Schuette, Manfred (Bayer A.-G. , Fed. Rep. Ger.). Ger. Offen. DE 3317823 A1 22 Nov 1984, 30 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: A01N053-00; A01N037-02; A01N037-04. APPLICATION: DE 83-3317823 17 May 1983. DOCUMENT TYPE: Patent CA Section: 5 (Agrochemical Bioregulators) Mono- or dicarboxylic acid esters, b.p. >250° synergize the insecticidal activity of the pyrethroids I (R and R1 = Br, Cl, or Me; R2 = H or CN; R3 = substituted Ph or PhO). Thus, in petri dish expts., a compn. contg. 0.006% by wt. fenfluthrin [75867-00-4] and 0.0006% by wt. diisononyl phthalate [28553-12-0] had a synergistic knock-down effect on Musca domestica.
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