Insecticidal N' substituted-N-N'-disubstituted-hydrazines

Organic compounds -- part of the class 532-570 series – Organic compounds – Amino nitrogen containing

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

564150, 564 36, 564 35, 564 81, 564 12, 564151, 564148, 564 74, 558415, 558 58, 558 10, 558273, 558404, 558 17, 558275, 558 6, 560138, 560 34, 560251, 560163, 560 27, 560221, 560 29, 560 30, 560 32, 560 31, 549553, 549436, 549496, 549487, 549 72, 549494, 549 65, 549484, 549546, 549419, 544406, 544335, 544224, C07C24100

Patent

active

051170574

ABSTRACT:
This invention relates to insecticidal compositions containing N'-substituted-N,N'-disubstitutedhydrazines, methods of using such compositions and N'-substituted-N, N'-disubstitutedhydrazines. Specifically, the invention relates to insect growth regulating compositions, and methods of using such compositions, which include compounds having a nucleus of the formula ##STR1## where A', B', D and J are independently any atom or group of atoms; where E is a tertiary carbon containing organic radical, a haloalkyl having a total of at least four carbon and halogen atoms but not more than six halogen atoms, or a non-tertiary carbon containing non-haloalkyl organic or organometallic radical having at least five atoms other than hydrogen, oxygen and halogen, and is attached to the nitrogen shown in the formula by a carbon-to-nitrogen single bond; where one G.sub.1 is C, N, O and S, and both G.sub.2 's and the other G.sub.1 are carbon; or one G.sub.2 is S or P, and both G.sub.1 's and the other G.sub.2 are carbon; where the bonds shown as - - - are independently single or double bonds; where the A'-?-G.sub.1 and G.sub.1 -?-B' bonds are independently single bond, double bonds or aromatic bonds; where organic radical is a radical comprising at least one carbon atom, but no metal atoms; where organometallic radical is a radical containing a carbon-to-metal bond; or an agronomically acceptable salt thereof; and with the provisos discussed infra.

REFERENCES:
patent: 2758054 (1956-08-01), Smith et al.
patent: 3092660 (1963-06-01), Gutmann et al.
patent: 3228833 (1966-01-01), Crounse et al.
patent: 3250764 (1986-05-01), Schmidt et al.
patent: 3636112 (1972-01-01), Draber et al.
patent: 3652533 (1972-03-01), Roueche
patent: 3660426 (1972-05-01), Cale et al.
patent: 3699111 (1972-10-01), Kaugars
patent: 3737533 (1973-06-01), Moon et al.
patent: 3745215 (1973-07-01), Kaugars
patent: 3746760 (1973-07-01), Sheppard et al.
patent: 3748356 (1973-07-01), Wellinga et al.
patent: 3773830 (1973-11-01), Dexter
patent: 3786094 (1974-01-01), Perronnet et al.
patent: 3809703 (1974-05-01), Kaugars
patent: 3821261 (1974-06-01), Kaugars
patent: 3824233 (1974-07-01), Friedman
patent: 3834892 (1974-09-01), Moon et al.
patent: 3867449 (1975-02-01), Moore
patent: 3870505 (1975-03-01), Kaugars
patent: 3879542 (1975-04-01), Kaugars
patent: 3884874 (1975-05-01), Rosenberger et al.
patent: 3897559 (1975-07-01), Friedman
patent: 3932660 (1976-01-01), Moore
patent: 3989842 (1976-11-01), Wellinga et al.
patent: 4007165 (1977-02-01), MacLeay et al.
patent: 4008217 (1977-02-01), Moon et al.
patent: 4008273 (1977-02-01), MacLeay et al.
patent: 4017540 (1977-04-01), Kaugars et al.
patent: 4018645 (1977-04-01), Takahashi et al.
patent: 4052362 (1977-10-01), Yoshikawa et al.
patent: 4062934 (1977-12-01), Tilly et al.
patent: 4071633 (1978-01-01), Aoki et al.
patent: 4189482 (1980-02-01), Truener et al.
patent: 4198434 (1980-04-01), Bergman et al.
patent: 4203932 (1980-05-01), Brown
patent: 4258059 (1981-03-01), Auerbach et al.
patent: 4268511 (1981-05-01), Baronnet et al.
patent: 4317741 (1982-03-01), Lederle et al.
patent: 4357351 (1982-11-01), Fancher et al.
patent: 4508734 (1985-04-01), Lange et al.
patent: 4533676 (1985-08-01), Sirrenberg et al.
patent: 4547524 (1985-10-01), Kaneko et al.
patent: 4550204 (1985-10-01), Von Gentzkow et al.
patent: 4551472 (1985-11-01), D'Silva
patent: 4564611 (1986-01-01), Stahler et al.
57 J. Pharm. Sci., 2011-2012 (1968).
Chemical Abstracts, 95:132148a (1981).
Chemical Abstracts, 85:142768k (1976).
Chemical Abstracts, 82:39589s (1975).
25 Aust. J. Chem., 523-529 (1972).
61 Helv. Chim. Acta, 1477-1510 (1978).
44 J.A.C.S., 2556-2567 (1922).
44 J.A.C.S., 1557-1564 (1922).
48 J.A.C.S., 1030-1035 (1926).
27 Bull. Chem. Soc. Japan, 624-627 (1954).
J. Chem. Soc. (C), 1531- 1536(1966).
56B Chem. Berichte, 954-962(1923).
590 Annalen der Chemie, 1-36(1954).
J. Chem. Soc., 4191-4198(1952).
32 Zhur. Obs. Khim., 2806-2809 (1962).
17 Acta. Chem. Scand., 95-102(1963).
25 Zhur. Obs. Khim., 1719-1723(1955).
J. Chem. Soc., 4793-4800(1974).
36 J. Prakt. Chem., 197-201(1967).
26 J.O.C., 4336-4340 (1961).
41 J.O.C., 3763-3765 (1976).
94 J.A.C.S., 7406-7416 (1972).
43 J.O.C., 808-815 (1978).
39 J. Econ. Ent., 416-417 (1946).
20 J. Agr. Food Chem., 888-891 (1972).
21 J. Agr. Food Chem., 647-650 (1973).
24 Journal of Medicinal Chemistry, 532-538 (1981).
Friedman, A. et al., "The Photolysis of Benzoyl Chloride (2,4,6-Trichlorophenyl)hydrazone," Pest.Chem., Proc. Int.IUPAC Congr.Pest.Chem., 3rd, 298-301.
Chemical Abstracts, 93:94943e (1980).
Chemical Abstracts, 73:3623y (1970).
Chemical Abstracts, 96:99275k (1982).
Chemical Abstracts, 65:8814a (1966).
Chemical Abstracts, 79:122571p (1973).
Chemical Abstracts, 77:126648a (1972).
13 Aldrichimica Acta., 33-40 (1980).
8 J. Pharm. Sci. U.A.R., 181-186 (1967).
23 J. Agric. Food Chem., 1084-1088 (1975).
48 J. Org. Chem., 2287- 2289 (1983).
92 Bull. Soc. Chim. Belg., 229-232 (1983).
48 Canadian Journal of Chemistry, 81-88 (1970).
Bentley, T. et al., "Aspects of Mass Spectra of Organic Compounds, Part XI, Rearrangements in Benzoylhydrazines," J. Chem. Soc., Perkin I, 449-453 (1973).
40 J. Org. Chem., 19-24 (1975).
44 J. Org. Chem., 2957-2961 (1979).
20 J. Agr. Food Chem., 1187-1190 (1972).
Chemical Abstracts, 77:34128c (1972).
28 Aust. J. Chem., 133-141 (1975).
88 J.A.C.S., 4677-4681 (1966).
Chemical Abstracts, 73:77209q (1970).
Chemical Abstracts, 83:178784k (1975).
Chemical Abstracts, 90:130606w (1979).
Chemical Abstracts, 84:150168j (1976).
37 Tetrahedron Letters, 3575-3578 (1979).
46 J. Org. Chem., 83-89 (1980).
Marchetti, L., "Reaction of Cyclohexanone Enamines with Diacyldi-imides," J. Chem. Soc. Perkin II, 382-390 (1978).
51 Can. J. Chem., 1587-1597 (1973).

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Insecticidal N' substituted-N-N'-disubstituted-hydrazines does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Insecticidal N' substituted-N-N'-disubstituted-hydrazines, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Insecticidal N' substituted-N-N'-disubstituted-hydrazines will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-421684

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.