NL7300886A - Herbicidal 3-substd -uracil-phenol complexes - Google Patents

Herbicidal 3-substd -uracil-phenol complexes

Info

Publication number
NL7300886A
NL7300886A NL7300886A NL7300886A NL7300886A NL 7300886 A NL7300886 A NL 7300886A NL 7300886 A NL7300886 A NL 7300886A NL 7300886 A NL7300886 A NL 7300886A NL 7300886 A NL7300886 A NL 7300886A
Authority
NL
Netherlands
Prior art keywords
substd
alkyl
opt
cycloalkyl
cycloalkenyl
Prior art date
Application number
NL7300886A
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed filed Critical
Priority to NL7300886A priority Critical patent/NL7300886A/en
Publication of NL7300886A publication Critical patent/NL7300886A/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/20—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D239/22—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to ring carbon atoms

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Herbicidal 3-substd.-uracil-phenol complexes: Z = H, Br, Cl, NO2, 1-3C alkyl or alkoxy Y = Cl or 1-3C alkyl m = 1-5 Either (A) p = 1 or 2 R1 = 1-10C alkyl, 1-8C substd. alkyl, 5-10C aryl, substd. Ph, 5-13C aralkyl opt. substd., 3-8C alkenyl or alkynyl, 3-12C cycloalkyl opt. substd., 4-12C cycloalkenyl opt. substd., 4-13C cycloalkylalkyl, 5-13C cycloalkenylalkyl, 5-14C (substd.-cycloalkyl)alkyl, 5-14C (substd.-cycloalkenyl)alkyl, CN R2 = Cl, F, Br, I, Me, Et, Pr, Bu, MeO, EtO, PrO, BuO, NO2, 2-6C alkoxymethyl, 1-6C hydroxyalkyl, 3-6C alkenyl, SCN, CN, HSCH2, 1-4C alkylthio, bromoethyl, FCH2, ClCH2, MeSCH2, PhSCH2, COOH.CH2SCH2. R3 = Me R4 = H (B) p = 1 or 2 R1 = 3-12C cycloalkyl opt. substd., 4-12C cycloalkenyl opt. substd., 4-13C cycloalkylalkyl, 4-13C cycloalkenylalkyl, 4-13C (substd.-cycloalkyl)alkyl, 4-13C (substd.-cycloalkenylalkyl) R2 = R4=H R3 = 1-5C alkyl (C) p = 1/2, 1 or 2 R1 = 1-10C alkyl opt. substd., 6-14C aryl opt. substd., 7-15C arallyl, 3-10C alkynyl or alkenyl, 3-12C cycloalkyl opt. substd., 4-12C cycloalkenyl opt. substd., 4-13C cycloalkylalkyl, 5-13C cycloalkenylalkyl, 5-14C (substd.-cycloalkyl)alkyl, 5-14C (subst.- cycloalkenyl)alkyl, 2-10C dialkylamino, CN, 1-10C alkoxyR2+R3 = (CH2)n where n = 3,4,5 R4 = H (D) p = 1 or 2 R1 = 1-10C alkyl opt. substd., 5-14C aryl opt. substd., 5-15C aralkyl opt. substd., 3-10C alkenyl or alkynyl, 3-12C cycloalkyl opt. substd., 4-12C cycloalkenyl opt. substd., 4-13C cycloalkylalkyl, 5-13C cycloalkenylalkyl, 5-14C (substd.-cycloalkyl)alkyl, 5-14C (substd.-cycloalkenyl) alkyl, 2-10C dialkylamino, CN, 1-10C alkoxy. R2 = H, Cl, F Br, I, Me, Et, Pr, Bu, MeO, EtO, PrO BuO, NO2, 2-6C alkoxymethyl, 1-6C hydroxyalkyl, 3-6C alkenyl, SCN, CN, HSCH2, 1-4C alkylthio, MeSCH2, ClCH2, BrCH2, FCH2, PhSCH2, COOH.CH2SCH2. With the proviso that when R2=H, R1=cycloalkyl, cycloalkenyl, cycloalkylalkyl or cycloalkenylalkyl R3 = R4=H or (E) R1 = 1-10C alkyl opt. substd., 5-14C aryl, 6-14C substd. aryl, 5-15C aralkyl, 7-15C substd. aralkyl, 3-10C alkenyl or alkynyl, 3-12C cycloalkyl opt. substd, 4-12C cycloalkenyl opt. substd., 4-13C cycloalkylalkyl, 5-13C cycloalkenylalkyl, 5-14C (substd.-cycloalkyl)-alkyl, 5-14C (substd.-cycloalkenyl)alkyl, 2-10C dialkylaminoalkyl, CN, 1-10C alkoxy R2 = as defined under (D) R3 = H or Me R4 = 1-6C alkyl, 1-6C acyl opt. substd.
NL7300886A 1973-01-22 1973-01-22 Herbicidal 3-substd -uracil-phenol complexes NL7300886A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
NL7300886A NL7300886A (en) 1973-01-22 1973-01-22 Herbicidal 3-substd -uracil-phenol complexes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL7300886A NL7300886A (en) 1973-01-22 1973-01-22 Herbicidal 3-substd -uracil-phenol complexes

Publications (1)

Publication Number Publication Date
NL7300886A true NL7300886A (en) 1973-04-25

Family

ID=19818053

Family Applications (1)

Application Number Title Priority Date Filing Date
NL7300886A NL7300886A (en) 1973-01-22 1973-01-22 Herbicidal 3-substd -uracil-phenol complexes

Country Status (1)

Country Link
NL (1) NL7300886A (en)

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