104040-78-0

Usage

Uses

Herbicide.

InChI:InChI=1/C13H12F3N5O5S/c1-25-8-6-9(26-2)19-11(18-8)20-12(22)21-27(23,24)10-7(13(14,15)16)4-3-5-17-10/h3-6H,1-2H3,(H2,18,19,20,21,22)

Upstream product

• 89392-03-0 O-phenyl N-(4,6-dimethoxypyrimidin-2-yl)carbamate 
• 104040-76-8 3-(trifluoromethyl)-2-pyridinesulfonamide 
• 111923-83-2 4,6-dimethoxypyrimidin-2-ylcarbamoyl chloride 
• 111284-03-8 2-isocyanato-4,6-dimethoxypyrimidine 

Downstream Products

• 104040-76-8 3-(trifluoromethyl)-2-pyridinesulfonamide 
• 181313-25-7 3-(trifluoromethyl)-2-pyridylsulfonylmethylcarbamate 
• 178403-35-5 N-(4,6-dimethoxypyrimidin-2-yl)-N-[3-(trifluoromethyl)-2-pyridinyl]urea 

Related news

Flazasulfuron (cas 104040-78-0) behavior in a soil amended with different organic wastes07/28/2019

We studied the flazasulfuron behavior in a soil amended with three organic wastes (municipal solid waste, MSW, poultry manure, PM, and cow manure, CM) and their influence both on its mobility and on the soil’s biochemical properties (soil humus-enzymatic complexes, soil microbial biomass-C and ...detailed

Relevant academic research and scientific papers

METHOD FOR PRODUCING PYRIMIDINE COMPOUND

To provide a method for producing pyrimidine compound useful as an intermediate for agricultural chemicals or pharmaceuticals, which is simple in operation, presents high yield and produces only a small amount of by-products. The method comprises reacting a compound represented by the formula (I) with a compound represented by the formula (II) in the presence of a pyridine compound to produce a compound represented by the formula (III), a compound represented by the formula (IV) or their mixture.

Method for producing a solid herbicide formulation

The invention relates to a method for producing a solid herbicide formulation containing a) a herbicide from the group of sulfonylurea, or the salts thereof which are useful in the agricultural domain, b) optionally at least one other herbicide, c) optionally a safener, and d) at least one formulation adjuvant. A suspension is formed in water, consisting of the sulfonylurea a), optionally at least one other herbicide b), optionally a safener c) and at least one formulation adjuvant d). The suspension is adjusted to a pH value between 6.5 and 8 by adding an acid or a base, and is then dried to obtain the solid formulation.

Non-aqueous or low-water suspension concentrates of mixtures of active compounds for crop protection

The invention relates to stable liquid and highly effective suspension concentrates comprisinga) one or more solid herbicidally active compounds from the group of the sulfonylureas in suspended form,b) one or more active compounds which are partially or completely dissolved in component c),c) an organic solvent or solvent mixture,d) one or more nonionic emulsifiers,e) optionally one or more ionic emulsifiers,f) optionally one or more thickeners or thixotropic agents and no water or up to 30 percent by weight of water in dissolved form.

N-phenylpyrrolidines

The 1-(3,5-bis-trifluoromethylphenyl)-2-thioxopyrrolidine-4-carboxylic acid derivatives of the formula I below are suitable for protecting crop plants against the phytotoxic action of herbicides and for regulating the plant growth. The 1-(3,5-bis-trifluoromethylphenyl)-2-thioxopyrrolidine-4-carboxylic acid derivatives are those of the formula I STR1 wherein A is --COOR1, --COSR1, --COO? M≈, --CONR2 R3 or --COCl; R1 is hydrogen, C1 -C4 alkyl, C2 -C6 alkenyl or C2 -C6 alkynyl; R2 and R3 independently of one another are hydrogen, C1 -C4 alkyl or C3 -C7 cycloalkyl; or R2 and R3 together with the nitrogen atom to which they are bonded are a saturated 3- to 7-membered heterocycle which can contain an additional hetero atom selected from the group comprising O, N and S and which is unsubstituted or up to trisubstituted by C1 14 C4 alkyl; and M≈ is the equivalent of an alkali metal cation or an alkaline earth metal cation or HN≈ (R2)3, and their isomers in optically pure or enriched form.