Tebufenpyrad

CAS : 119168-77-3

Ref. 3D-FT28018

Informations sur le produit

• Nom: Tebufenpyrad
• Synonymes: 4-Chloro-N-[[4-(1,1-dimethylethyl)phenyl]methyl]-3-ethyl-1-methyl-1H-pyrazole-5-carboxamideAC 801757Fenpyrad, 1H-Pyrazole-5-carboxamide, 4-chloro-N-[[4-(1,1-dimethylethyl)phenyl]methyl]-3-ethyl-1-methyl-, 4-Chloro-N-(4-tert-butylbenzyl)-3-ethyl-1-methyl-1H-pyrazole-5-carboxamide, 4-chloro-N-(4-(1,1-dimethylethyl)phenyl)methyl-3-ethyl-1-methyl-1H-pyrazole-5-carboxamide, Ac 801757, Comanche, Fenpyrad, Masai, Mk 239, N-(4-tert-Butylbenzyl)-4-chloro-3-ethyl-1-methylpyrazole-5-carboxamide, N-(4-tert-butylbenzyl)-4-chloro-3-ethyl-1-methyl-1H-pyrazole-5-carboxamide, N-(4-tert-butylbenzyl)-4-chloro-3-ethyl-1-methyl-5-pyrazolemethylamide, Oscar, Pyranica

Description

Tebufenpyrad is a fungicide with acylation activity. It is also a matrix effect modifier and synergist for other fungicides, such as thiophanate-methyl, chlorothalonil, and propiconazole. Tebufenpyrad is used in the treatment of plant diseases caused by fungi that are resistant to other fungicides. Tebufenpyrad has been shown to be an effective fungicide against strains of fungi resistant to other chemical classes of fungicides. Tebufenpyrad inhibits the synthesis of DNA by binding to the enzyme RNA polymerase II, which prevents transcription and replication. The inhibition of RNA polymerase II leads to a reduction in mRNA synthesis, disrupting protein synthesis and cell division. This product also has genotoxic activity, which may be due to its ability to induce apoptosis.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 333.86 g/mol
• Formule: C₁₈H₂₄ClN₃O
• Degré de pureté: Min. 95%
• Couleur/Forme: White Powder
• InChI: InChI=1S/C18H24ClN3O/c1-6-14-15(19)16(22(5)21-14)17(23)20-11-12-7-9-13(10-8-12)18(2,3)4/h7-10H,6,11H2,1-5H3,(H,20,23)
• Code InChI: InChIKey=ZZYSLNWGKKDOML-UHFFFAOYSA-N
• SMILES: CCc1nn(C)c(C(=O)NCc2ccc(C(C)(C)C)cc2)c1Cl