Abstract

Provided are m-diamide compounds and a preparation method therefor and the use thereof. The m-diamide compounds have a structure represented by formula I. The m-diamide compounds of the present invention can have a high insecticidal activity at a low dose and take effect rapidly, can exert the insecticidal activity one day after application, can achieve a high insecticidal activity within three days, and have a good fast-acting property; moreover, due to the good effect at a low dose, the m-diamide compounds can reduce the damage to plants and human beings caused by excessive drug concentrations, enable less drug residue to be generated during application which is more conducive to environmental protection, and have broad application prospects.

IPC Classes  ?

• A01N 37/18 - Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N, e.g. carboxylic acid amides or imidesThio-analogues thereof
• C07C 237/42 - Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
• C07C 255/50 - Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings

Abstract

A pharmaceutical composition containing an M-diamide compound and an application thereof. The pharmaceutical composition comprises an active ingredient A and an active ingredient B, the active ingredient A is an M-diamide compound having a structure represented by formula I, and the active ingredient B is any one or a combination of two of an insecticide such as thiamethoxam and a fungicide such as prothioconazole. The composition containing the active ingredient A and the active ingredient B has unique effects such as synergy, expanding the prevention spectrum, and controlling spreader insects, and may effectively prevent multiple types of pests and diseases in crops such as rice, corn, wheat, vegetables, fruit trees, flowers, oil, and sugar, and horticulture and forestry.

IPC Classes  ?

• A01N 37/18 - Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N, e.g. carboxylic acid amides or imidesThio-analogues thereof
• A01N 37/34 - Nitriles
• A01N 43/836 - 1,2,4-Oxa(thia)diazolesHydrogenated 1,2,4-oxa(thia)diazoles
• A01P 7/04 - Insecticides
• C07C 237/42 - Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
• C07C 255/50 - Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
• C07D 271/06 - 1,2,4-OxadiazolesHydrogenated 1,2,4-oxadiazoles

Abstract

Provided are a pharmaceutical composition comprising a meta-diamide compound and the use thereof. The pharmaceutical composition includes an active ingredient A and an active ingredient B, wherein the active ingredient A is a meta-diamide compound having a structure as shown in formula I, and the active ingredient B is a combination of any one or two of other insecticides or fungicides. The composition comprising the active ingredient A and the active ingredient B has unique effects of synergy, managing resistant pests, expanding spectrum of activity and controlling poisonous insects, which can effectively control a variety of diseases and insect pests of rice, corn, wheat, vegetables, fruit trees, flowers, oil plants, sugar crops and other crops, as well as diseases and insect pests in horticulture and forestry.

IPC Classes  ?

• A01N 37/18 - Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N, e.g. carboxylic acid amides or imidesThio-analogues thereof
• A01N 37/34 - Nitriles
• A01N 43/836 - 1,2,4-Oxa(thia)diazolesHydrogenated 1,2,4-oxa(thia)diazoles
• A01P 7/04 - Insecticides
• C07C 237/42 - Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
• C07C 255/50 - Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
• C07D 271/06 - 1,2,4-OxadiazolesHydrogenated 1,2,4-oxadiazoles

Abstract

A pharmaceutical composition containing a meta-diamide compound and use thereof. The pharmaceutical composition comprises an active ingredient A and an active ingredient B. The active ingredient A is a meta-diamide compound having a structure as shown in formula I, and the active ingredient B comprises any one or a combination of two of other bactericides, insecticides or acaricides. The active ingredient A and the active ingredient B have a synergistic effect, the use amount of the composition is greatly reduced compared with that of an insecticide having a single active ingredient, the control effect is greatly improved, and the control profile is enlarged. Said composition can be applied to various plant diseases and insect pests of crops such as vegetables, fruit trees, flowers, cereals, oil plants and sugar plants as well as those in the field of horticulture and forestry, and can delay the development of drug resistance.

IPC Classes  ?

• A01N 37/46 - N-acyl derivatives
• A01N 41/10 - SulfonesSulfoxides
• A01N 43/836 - 1,2,4-Oxa(thia)diazolesHydrogenated 1,2,4-oxa(thia)diazoles
• A01N 51/00 - Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring
• A01N 57/16 - Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals
• A01N 43/90 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
• A01N 57/28 - Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-nitrogen bonds containing acyclic or cycloaliphatic radicals
• A01N 43/76 - 1,3-OxazolesHydrogenated 1,3-oxazoles
• A01N 43/56 - 1,2-DiazolesHydrogenated 1,2-diazoles
• A01N 43/36 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
• A01P 7/04 - Insecticides
• A01P 7/02 - Acaricides

Abstract

A drug composition containing an M-diamide compound and application of the drug composition. The drug composition comprises an effective constituent A and an effective constituent B; the effective constituent A is the M-diamide compound having a structure shown as formula I, and the effective constituent B comprises any one or combinations of two of other insecticides. The composition containing the effective constituent A and the effective constituent B has unique functions such as a synergistic effect, control of resistant pests, expansion of an activity spectrum, and control of virus spreading insects, and can effectively control multiple diseases and pests on crops such as rice, corn, wheat, vegetables, fruit trees, flowers, oil plants, and sugar crops, and horticulture and forestry.

IPC Classes  ?

• A01N 37/18 - Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N, e.g. carboxylic acid amides or imidesThio-analogues thereof
• A01N 37/34 - Nitriles
• A01N 43/836 - 1,2,4-Oxa(thia)diazolesHydrogenated 1,2,4-oxa(thia)diazoles
• A01P 7/04 - Insecticides
• C07C 237/42 - Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
• C07C 255/50 - Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
• C07D 271/06 - 1,2,4-OxadiazolesHydrogenated 1,2,4-oxadiazoles

Abstract

A pharmaceutical composition containing an m-diamide compound and an application thereof. The pharmaceutical composition comprises an active component A and an active component B, wherein the active component A is the m-diamide compound having a structure represented by formula I, and the active component B is a combination of any one or two of other pesticides or bactericides. The composition containing the active component A and the active component B has the unique effects of synergistic interaction, resistant pest control, enlargement of an activity spectrum, virus-transmitting insect control and the like, and can effectively prevent and treat various diseases and insect pests on crops such as rice, corn, wheat, vegetables, fruit trees, flowers, oil materials, sugar materials and the like as well as gardening and forestry.

IPC Classes  ?

• A01N 37/18 - Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N, e.g. carboxylic acid amides or imidesThio-analogues thereof
• A01N 37/34 - Nitriles
• A01N 43/836 - 1,2,4-Oxa(thia)diazolesHydrogenated 1,2,4-oxa(thia)diazoles
• A01P 7/04 - Insecticides
• C07C 237/42 - Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
• C07C 255/50 - Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
• C07D 271/06 - 1,2,4-OxadiazolesHydrogenated 1,2,4-oxadiazoles

Abstract

Provided are m-diamide compounds and a preparation method therefor and the use thereof. The m-diamide compounds have a structure represented by formula I. The m-diamide compounds of the present invention can have a high insecticidal activity at a low dose and take effect rapidly, can exert the insecticidal activity one day after application, can achieve a high insecticidal activity within three days, and have a good fast-acting property; moreover, due to the good effect at a low dose, the m-diamide compounds can reduce the damage to plants and human beings caused by excessive drug concentrations, enable less drug residue to be generated during application which is more conducive to environmental protection, and have broad application prospects.

IPC Classes  ?

• A01N 37/18 - Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N, e.g. carboxylic acid amides or imidesThio-analogues thereof
• A01N 37/34 - Nitriles
• A01N 37/46 - N-acyl derivatives
• A01N 37/48 - Nitro-carboxylic acidsDerivatives thereof
• A01N 41/10 - SulfonesSulfoxides
• A01N 43/836 - 1,2,4-Oxa(thia)diazolesHydrogenated 1,2,4-oxa(thia)diazoles
• A01P 7/04 - Insecticides
• C07C 237/42 - Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
• C07C 255/50 - Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
• C07D 271/06 - 1,2,4-OxadiazolesHydrogenated 1,2,4-oxadiazoles

Abstract

Provided are m-diamide compounds and a preparation method therefor and the use thereof. The m-diamide compounds have a structure represented by formula I. The m-diamide compounds of the present invention can have a high insecticidal activity at a low dose and take effect rapidly, can exert the insecticidal activity one day after application, can achieve a high insecticidal activity within three days, and have a good fast-acting property; moreover, due to the good effect at a low dose, the m-diamide compounds can reduce the damage to plants and human beings caused by excessive drug concentrations, enable less drug residue to be generated during application which is more conducive to environmental protection, and have broad application prospects.

IPC Classes  ?

• C07C 237/42 - Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
• C07C 255/50 - Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
• C07D 271/06 - 1,2,4-OxadiazolesHydrogenated 1,2,4-oxadiazoles
• A01N 37/18 - Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N, e.g. carboxylic acid amides or imidesThio-analogues thereof
• A01N 37/46 - N-acyl derivatives
• A01N 37/34 - Nitriles
• A01N 37/48 - Nitro-carboxylic acidsDerivatives thereof
• A01N 41/10 - SulfonesSulfoxides
• A01N 43/836 - 1,2,4-Oxa(thia)diazolesHydrogenated 1,2,4-oxa(thia)diazoles
• A01P 7/04 - Insecticides

Abstract

An anhydrous heat transfer medium, comprising any one or a combination of at least two of cis-1-chloro-3,3,3-trifluoropropene, cis-1,1,1,4,4,4-hexafluorobutene or perfluorobutane methyl ether. The heat transfer medium does not require an external device to perform work on the heat transfer medium during a heat transfer process, and is anhydrous, non-combustible, non-conductive and environmentally friendly.

IPC Classes  ?

• C08J 9/14 - Working-up of macromolecular substances to porous or cellular articles or materialsAfter-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic