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4-Methyl-3-(methylthio)-5-phenyl-4H-1,2,4-triazole, also known as 4M3M5P4HT, is a chemical compound belonging to the 1,2,4-triazole family. It features a 1,2,4-triazole ring structure with a methyl group at the 4-position, a methylthio group at the 3-position, and a phenyl group at the 5-position. 4-METHYL-3-(METHYLTHIO)-5-PHENYL-4H-1,2,4-TRIAZOLE is primarily used as a fungicide in various agricultural applications, particularly for the control of powdery mildew in crops. Its chemical formula is C10H11N3S, and it has a molecular weight of 209.29 g/mol. The compound is known for its effectiveness in protecting plants from fungal infections, making it a valuable tool in modern agriculture.

25812-76-4

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25812-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25812-76-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,1 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25812-76:
(7*2)+(6*5)+(5*8)+(4*1)+(3*2)+(2*7)+(1*6)=114
114 % 10 = 4
So 25812-76-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3S/c1-13-9(11-12-10(13)14-2)8-6-4-3-5-7-8/h3-7H,1-2H3

25812-76-4Relevant academic research and scientific papers

Triazolyl azabicyclo[3.1.0]hexanes: A class of potent and selective dopamine D3 receptor antagonists

Bonanomi, Giorgio,Braggio, Simone,Capelli, Anna Maria,Checchia, Anna,Di Fabio, Romano,Marchioro, Carla,Tarsi, Luca,Tedesco, Giovanna,Terreni, Silvia,Worby, Angela,Heibreder, Christian,Micheli, Fabrizio

experimental part, p. 705 - 715 (2011/01/05)

Herein we report a detailed description of the structure-activity relationships for a novel series of "C-linked" 1,2,4- triazolylazabicyclo[3.1.0]hexanes. These derivatives are endowed with very high in vitro affinity and selectivity for the dopamine Dsu

5-Aryl-3-(alkylthio)-4H-1,2,4-triazoles as selective antagonists of strychnine-induced convulsions and potential antispastic agents

Kane,Staeger,Dalton,Miller,Dudley,Ogden,Kehne,Ketteler,McCloskey,Senyah,Chmielewski,Miller

, p. 125 - 132 (2007/10/02)

Selected examples from three series of isomeric (alkylthio)-1,2,4- triazoles were prepared and examined for anticonvulsant activity versus strychnine-, maximal-electroshock-, pentylenetetrazole-, and 3- mercaptopropionic-acid-induced seizures in mice. A n

3-aryl-5-alkylthio-4H-1,2,4-triazoles

-

, (2008/06/13)

This invention relates to novel sulfone and sulfoxide derivatives of 3-aryl-5-alkylthio-4H-1,2,4-triazoles and to the use of 3-aryl-5-alkylthio-, alkylsulfinyl- and alkylsulfonyl-4H-1,2,4-triazoles in the treatment of patients suffering from convulsant seizures.

3-aryl-5-alkylthio-4H-1,2,4-traizoles for treatment of hyperreflexia due to spinal trauma

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, (2008/06/13)

This invention relates to the use of 3-aryl-5-alkylthio-4H-1,2,4-triazoles and the corresponding alkylsulfinyl- and alkylsulfonyl-4H-1,2,4-triazoles in the treatment of patients suffering from chronic hyperreflexia due to spinal trauma.

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