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2-chloro-4-fluoro-5-(3,6-dihydro-3-methyl-2,6-dioxo-4-trifluoromethyl-1(2H)-pyrimidinyl)thiophenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

353292-92-9

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353292-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 353292-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,3,2,9 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 353292-92:
(8*3)+(7*5)+(6*3)+(5*2)+(4*9)+(3*2)+(2*9)+(1*2)=149
149 % 10 = 9
So 353292-92-9 is a valid CAS Registry Number.

353292-92-9Downstream Products

353292-92-9Relevant academic research and scientific papers

Synthesis of Cyclopropyl Ester and Amide Substituted Pyrimidinediones as Protoporphyrinogen Oxidase-Inhibiting Herbicides

Choi, Jong-Soo,Kwon, Young Bin,Lee, Kye Hwan,Lee, Won Hyung,Seu, Young-Bae

, p. 420 - 428 (2021/01/18)

The protoporphyrinogen oxidase (PPO) enzyme is involved in the biosynthesis of chlorophyll and is an important target in research for development of new herbicides. In this study, new pyrimidinedione compounds with thioester tail group containing cyclopropyl moiety are synthesized from the commercially available 2-(1-(mercaptomethyl)cyclopropyl)acetic acid. The herbicidal activity of the synthesized compounds is also evaluated. Most of the synthesized compounds exhibit herbicidal activities against both monocot and dicot weeds. In particular, 10a showed similar activity to the control material, Saflufenacil. And when against the monocot weeds, Echinochloa crusgalli and Digitaria sanguinalis, 10a shows superior activity to Saflufenacil.

SUBSTITUTED THIOPHENYL URACILS, SALTS THEREOF AND THE USE THEREOF AS HERBICIDAL AGENTS

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, (2021/04/02)

The invention relates to substituted thiophenyl uracils of general formula (I) or salts (I) thereof, wherein the groups in general formula (I) are as defined in the description, and to the use thereof as herbicides, in particular for controlling weeds and

Design and synthesis of acrylate and acrylamide substituted pyrimidinediones as potential PPO herbicides

Choi, Jong-Soo,Kim, Jung Hee,Kwon, Young Bin,Lee, Kye Hwan,Lee, Won Hyung,Maezono, Shizuka Mei Bautista,Seu, Young-Bae

, (2021/01/07)

PPO herbicides emerge to be widely use in the agricultural field and a focus of research to many scientists due to its environmentally-friendly properties. In lieu with this, this study presents acrylate and acrylamide substituted pyrimidinediones as PPO herbicide candidates. Most synthesized compounds exhibits herbicidal activities against both monocot and dicot weeds, especially, compound 5a which showed non-selective superior activity against the commercialized, Saflufenacil. Compound 5a was further tested for residual effect and showed promising results as shorter period is needed to cultivate the next crops. The synthesized acrylate and acrylamide substituted pyrimidinediones, especially, 5a could potentially be utilized in the development of commercial protoporphyrinogen oxidase inhibitors with further tests and studies.

SUBSTITUTED THIOPHENYL URACILS, SALTS THEREOF AND THE USE THEREOF AS HERBICIDAL AGENTS

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, (2020/11/27)

The invention relates to substituted thiophenyl uracils of general formula (I) or the salts (I) thereof, wherein the groups in general formula (I) are as defined in the description, and to the use thereof as herbicides, in particular for controlling weeds and/or weed grasses in crops of cultivated plants and/or as plant growth regulators for influencing the growth of crops of cultivated plants.

PROCESS FOR PREPARING 5-(3,6-DIHYDRO-2,6-DIOXO-4-TRIFLUOROMETHYL-1(2H)-PYRIMIDINYL)PHENYLTHIOL

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Paragraph 0044-0053, (2020/07/15)

The present invention relates to a method for preparing 5-(3,6-dihydro-2,6-dioxo-4-trifluoromethyl-1(2H)-pyrimidinyl) phenylthiol compounds in a reactor.

Uracil compounds and use thereof

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, (2008/06/13)

The present invention relates to an uracil compound of the formula [I]: [wherein, Q—R3represents a R3-substituted group of a 5-membered or 6-membered heterocyclic ring having one or two nitrogen selected from the group consisting of

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