Fluopyram - Moligand™,≥98% , CAS No.658066-35-4

CAS: 658066-35-4 Cat. No.: F304303 Peso molecular: 396.71 Número EC: 619-797-7

GRADE & PURITY Moligand™, ≥98%

Synonyms

n-[2-[3-chloro-5-(trifluoromethyl)-2-pyridinyl]ethyl]-2-trifluoromethylbenzamide | AE C656948 | AKOS027323805 | DTXSID9058151 | Fluopyram, PESTANAL(R), analytical standard | Fluopyram | N-[2-[3-Chloro-5-(trifluoromethyl)-2-pyridyl]ethyl]-2-(trifluoromethy

Storage

Conservar a 2-8°C,Protegido de la luz

Shipped In

Hielo húmedo

Descripción general

Fluopyram es un nuevo fungicida de piridiniletilbenzamida. Es muy eficaz en el control de una amplia variedad de patógenos como Botrytis spp., Sclerotinia spp. y Monilia spp., y también contra oídio y algunas enfermedades de manchas foliares en una amplia gama de cultivos.

Aplicación

Consulte el certificado de análisis del producto para obtener más información sobre la técnica instrumental adecuada. Póngase en contacto con el Servicio Técnico para obtener más ayuda

Specifications

Sinónimos

n-[2-[3-chloro-5-(trifluoromethyl)-2-pyridinyl]ethyl]-2-trifluoromethylbenzamide | AE C656948 | AKOS027323805 | DTXSID9058151 | Fluopyram, PESTANAL(R), analytical standard | Fluopyram | N-[2-[3-Chloro-5-(trifluoromethyl)-2-pyridyl]ethyl]-2-(trifluoromethy

Especificaciones y pureza

Moligand™, ≥98%

Mecanismos bioquímicos y fisiológicos

El fluopiram afecta al crecimiento fúngico en todas las fases, desde la germinación hasta la esporulación. Según diversos estudios, su modo de acción bioquímica se basa en la inhibición de la succinato deshidrogenasa (complejo II) presente en el hongo

Condiciones de almacenamiento de almacenamiento

Conservar a 2-8°C, Protegido de la luz

Enviado en

Hielo húmedo

Grado

Moligand™

Tipo de acción

INHIBITOR

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504766088
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504766088
• Sonrisas canónicas: C1=CC=C(C(=C1)C(=O)NCCC2=C(C=C(C=N2)C(F)(F)F)Cl)C(F)(F)F
• IUPAC Name: N-[2-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]ethyl]-2-(trifluoromethyl)benzamide
• InChIKey: KVDJTXBXMWJJEF-UHFFFAOYSA-N
• INCHI: 1S/C16H11ClF6N2O/c17-12-7-9(15(18,19)20)8-25-13(12)5-6-24-14(26)10-3-1-2-4-11(10)16(21,22)23/h1-4,7-8H,5-6H2,(H,24,26)
• Isómeros SMILES: C1=CC=C(C(=C1)C(=O)NCCC2=C(C=C(C=N2)C(F)(F)F)Cl)C(F)(F)F
• Peso molecular: 396.71
• Reaxy-Rn: 11323270
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11323270&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Trifluoromethylbenzenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Trifluoromethylbenzenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Trifluoromethylbenzenes
• Alternative Parents: Benzamides Benzoyl derivatives Pyridines and derivatives Aryl chlorides Heteroaromatic compounds Secondary carboxylic acid amides Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organofluorides Organochlorides Organic oxides Hydrocarbon derivatives Alkyl fluorides
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Trifluoromethylbenzene - Benzamide - Benzoic acid or derivatives - Benzoyl - Aryl chloride - Aryl halide - Pyridine - Heteroaromatic compound - Secondary carboxylic acid amide - Carboxamide group - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Alkyl fluoride - Organofluoride - Organochloride - Organohalogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Alkyl halide - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as trifluoromethylbenzenes. These are organofluorine compounds that contain a benzene ring substituted with one or more trifluoromethyl groups.
• External Descriptors: organochlorine compound - benzamides - pyridines - (trifluoromethyl)benzenes - benzamide fungicide

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (no humanos)

Botrytis cinerea (4183 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Light & Moisture sensitive
• Peso molecular: 396.710 g/mol
• XLogP3: 4.500
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 4
• Exact Mass: 396.046 Da
• Monoisotopic Mass: 396.046 Da
• Topological Polar Surface Area: 42.000 Ų
• Heavy Atom Count: 26
• Formal Charge: 0
• Complexity: 484.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Min Wang, Yajie Yue, Jingjing Zhang, Yifan Qin, Liyan Jia, Xu Jing.  (2024)  Dispersive liquid-liquid microextraction based on magnetic deep eutectic solvent for the determination of succinate dehydrogenase inhibitors in water, juice, wine, and vinegar.  JOURNAL OF FOOD COMPOSITION AND ANALYSIS,      [PMID:] [10.1016/j.jfca.2024.106411]

2. Yajie Yue, Yawen Zhang, Yulin Wang, Xiaoning Wei, Yong Fang, Kasim Sakran Abass, Shu Qin, Xu Jing.  (2025)  Sodium alginate-fortified emulsive liquid-liquid microextraction for detecting succinate dehydrogenase inhibitor fungicides in water, juice, and wine.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:40789397] [10.1016/j.ijbiomac.2025.146722]

3. Zhang Heng, Zhu Zhangling, Peng Mengqi, Liu Sijie, Gong Xiao, Chen Tian, Hu Qingwen, Li Linyun, Dun-zhu Zha-xi, Drol-ga Lha-zom, Sun Yi.  (2025)  Agricultural SDHIs Induce Azole Resistance in Aspergillus fumigatus via Mitochondrial Sdh1 Suppression.  MYCOPATHOLOGIA,  190  (5): (1-16).  [PMID:40952433] [10.1007/s11046-025-00992-0]

4. Longzhu Bao, Hexiang Wang, Yu Chen, Jie Deng, Fang Liu, Huailong Teng, Shaoyong Ke.  (2026)  Design of novel tryptamine-based SDHI fungicides inspired by rice phytoalexins: Antifungal activity evaluation and molecular mechanism.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:41629033] [10.1016/j.pestbp.2026.106965]