1,2,4,6-thiatriazine 1,1-dioxide ethers and their use

  • 1,2,4,6-thiatriazine 1,1-dioxide ethers and their use

    1,2,4,6-thiatriazine 1,1-dioxide ethers and their use

    1,2,4,6-Thiatriazine 1,1-dioxide ethers of the formula where R1, R2, R3, Y, Z and n have the meanings given in the description, are used for controlling undesirable plant growth.

  • 1,2,4,6-thiatriazine 1,1-dioxide ethers and their use

    1,2,4,6-thiatriazine 1,1-dioxide ethers and their use

    The present invention relates to 1,2,4,6-thiatriazine 1,1-dioxide ethers, herbicides which contain these compounds as active ingredients and their use for controlling undesirable plant growth. It is known that substituted 6H-1,2,4,6-thiatriazin-5-one 1,1-dioxide derivatives have a herbicidal action (German Laid-Open Applications DOS 2,508,832

  • 1,2,4,6-thiatriazin-1,1-dioxide ethers, process for their

    1,2,4,6-Thiatriazin-1,1-dioxide ethers, process for their

    1,2,4,6-Thiatriazine 1,1-dioxide ethers of the formula where R1, R2, R3, Y, Z and n have the meanings given in the description, are used for controlling undesirable plant growth.

  • 6h-1,2,4,6-thiatriazine-1,1-dioxides - basf aktiengesellschaft

    6H-1,2,4,6-Thiatriazine-1,1-dioxides - BASF Aktiengesellschaft

    We claim: 1. A 6H-1,2,4,6-thiatriazine-1,1-dioxide of the formula ##STR19## where R 1 is an alkyl, alkenyl or alkynyl radical of up to 10 carbon atoms, a cycloalkyl radical of 3 to 7 carbon atoms, a branched, saturated or unsaturated alkyl, alkenyl or alkynyl radical of 3 to 10 carbon atoms, a halogen-, alkoxy- or alkylmercapto-substituted straight-chain or branched alkyl, alkenyl or alkynyl

  • synthesis of 1,2,4,6-thiatriazine 1,1-dioxides. part iii

    Synthesis of 1,2,4,6-thiatriazine 1,1-dioxides. Part III

    We have recently reported methods for preparing the three possible isomeric forms of ring N substituted 3,5iamino-1,2,4,6-thiatriazine 1,1ioxides 1 2 We now wish to present some of the synthetic routes we have developed which give access to the 3-alkyl/aryl derivatives 1 and 2 of this ring system nd which complement and extend our procedure.

  • ep0170203a2 - 4h-pyrido(2,3-d)(1,3)oxazin-4-one derivatives

    EP0170203A2 - 4H-Pyrido(2,3-d)(1,3)oxazin-4-one derivatives

    4H-Pyrido [2,3-d] [1,3] oxazin-4-one derivatives of the formula <IMAGE> in which Y is oxygen or sulfur and R is one by halogen, haloalkyl, haloalkoxy, haloalkylmercapto, haloalkylsulfinyl or haloalkylsulfonyl substituted phenyl radical, processes for their manufacture and their use for combating undesirable plant growth.

  • gb1578963a - cyclic esters of 3,4-dihydroxy-thiophene-1,1

    GB1578963A - Cyclic esters of 3,4-dihydroxy-thiophene-1,1

    GB1578963A - Cyclic esters of 3,4-dihydroxy-thiophene-1,1-dioxide compounds and 3,4-dihydroxy-cyclopentadienone compounds and their use as intermediates - Google Patents

  • nc deq: glycol ethers

    NC DEQ: Glycol Ethers

    For more information related to glycol ether compounds, please contact: Jim Bowyer, Ph.D. (919)715-7484 (919)-715-0890 fax Use partial or complete CAS# or names to search for compounds and their synonyms.

  • cheminform: vol 21, no 37

    ChemInform: Vol 21, No 37

    ChemInform Abstract: Fluorine‐Containing Bioactive Heterocycles. Investigation of the Reactions of Fluorine‐Containing 3‐Hydrazino‐5H‐1,2,4‐triazino(5,6‐b)indoles with Carbon Disulfide and Synthesis of 2,3‐Dihydro‐1‐thioxo‐1,2,4‐triazolo(3,4‐c)‐1,2,4‐triazino(5,6‐b)indoles as Antibacterial Agents.

  • diazoxide

    Diazoxide

    Diazoxide was approved for medical use in the United States in 1973. It is on the World Health Organization's List of Essential Medicines, the safest and most effective medicines needed in a health system. It is available as a generic medication. In the United States as of 2019 it costs about US$1500 per month.

  • 21 cfr 176.180 - components of paper and paperboard

    21 CFR 176.180 - Components of paper and paperboard

    3,3,4,4-Tetrachlorotetrahydrothiophene-1,1-dioxide Tetrakis(hydroxymethyl)phosphonium sulfate (CAS Reg. No. 55566-30-8) Maximum use level of 84 mg/kg in the pulp slurry. The additive may also be added to water, which when introduced into the pulp slurry, results in a concentration in the pulp slurry not to exceed 84 mg/kg.

  • molbank | free full-text | 1-[5-(4-tolyl)-1,3,4-oxadiazol-2

    Molbank | Free Full-Text | 1-[5-(4-Tolyl)-1,3,4-oxadiazol-2

    1-[5-(4-Tolyl)-1,3,4-oxadiazol-2-yl]methanamine (3) has been successfully synthesized by reacting p-toluic hydrazide (1) and glycine (2) via the polyphosphoric acid condensation route. The course of the reaction was found to be high yielding (87%) and the title compound was spectroscopically characterized by UV-Vis, FTIR, DSC, 13C/1H-NMR, and sass spectrometric techniques.