Fluxapyroxad - ≥98% , CAS No.907204-31-3

CAS: 907204-31-3 Cat. No.: F412925 Summenformel: C₁₈H₁₂F₅N₃O Molekulargewicht: 381.3 EG-Nummer: 620-041-3

QUALITÄT & REINHEIT ≥98%

Synonyms

EN300-264529 | Fluxapyroxad 100 microg/mL in Acetonitrile | AKOS015963993 | UNII-7U8P4NAR2S | AKOS015895375 | 1ST000820 | Fluxapyroxad | potassium butyl xanthate | AS-36599 | Z1552164593 | DTXSID6058215 | AKOS027322014 | Q15632875 | 3-(difluoromethyl)-1-m

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Übersicht

Information

Fluxapyroxad, a broad-spectrum fungicide, is an inhibitor of the succinate dehydrogenase (SQR) enzyme.

Product Application:

Fluxapyroxad is a new generation carboxamide funugicide and its residues are found in food. Pesticide component.

Spezifikationen

Synonyme

EN300-264529 | Fluxapyroxad 100 microg/mL in Acetonitrile | AKOS015963993 | UNII-7U8P4NAR2S | AKOS015895375 | 1ST000820 | Fluxapyroxad | potassium butyl xanthate | AS-36599 | Z1552164593 | DTXSID6058215 | AKOS027322014 | Q15632875 | 3-(difluoromethyl)-1-m

Spezifikationen & Reinheit

≥98%

Biochemische und physiologische Mechanismen

Fluxapyroxad, a broad-spectrum fungicide, is an inhibitor of the succinate dehydrogenase (SQR) enzyme.

Storage

Store at -20°C

Verschickt in

Ice chest + Ice pads

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Aktionsart

INHIBITOR

Reinheit

≥98%

Namen und Kennungen

Pubchem Sid

488199037

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488199037

Kanonisches Lächeln

CN1C=C(C(=N1)C(F)F)C(=O)NC2=CC=CC=C2C3=CC(=C(C(=C3)F)F)F

IUPAC Name

3-(difluoromethyl)-1-methyl-N-[2-(3,4,5-trifluorophenyl)phenyl]pyrazole-4-carboxamide

InChIKey

SXSGXWCSHSVPGB-UHFFFAOYSA-N

INCHI

1S/C18H12F5N3O/c1-26-8-11(16(25-26)17(22)23)18(27)24-14-5-3-2-4-10(14)9-6-12(19)15(21)13(20)7-9/h2-8,17H,1H3,(H,24,27)

Isomere SMILES

CN1C=C(C(=N1)C(F)F)C(=O)NC2=CC=CC=C2C3=CC(=C(C(=C3)F)F)F

Molekulargewicht

381.3

Reaxy-Rn

15702063

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=15702063&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Klasse Benzene and substituted derivatives
      • Subclass Anilides

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: Benzene and substituted derivatives
• Subclass: Anilides
• Intermediate Tree Nodes: Not available
• Direct Parent: Aromatic anilides
• Alternative Parents: Biphenyls and derivatives Pyrazole-4-carboxamides Fluorobenzenes Aryl fluorides Vinylogous amides Heteroaromatic compounds Secondary carboxylic acid amides Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organofluorides Organic oxides Hydrocarbon derivatives Alkyl fluorides
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Aromatic anilide - Biphenyl - Pyrazole-4-carboxamide - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Azole - Heteroaromatic compound - Vinylogous amide - Pyrazole - Carboxamide group - Secondary carboxylic acid amide - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Alkyl fluoride - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Alkyl halide - Aromatic heteromonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as aromatic anilides. These are aromatic compounds containing an anilide group in which the carboxamide group is substituted with an aromatic group. They have the general structure RNC(=O)R', where R= benzene, and R = aryl group.
• External Descriptors: pyrazoles - biphenyls - aromatic amide - anilide fungicide - trifluorobenzene

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

Chemische und physikalische Eigenschaften

• Löslichkeit: DMSO (Slightly), Methanol (Slightly)
• Schmelzpunkt (°C): 156 - 158°C
• Molekulargewicht: 381.300 g/mol
• XLogP3: 3.700
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 4
• Exact Mass: 381.09 Da
• Monoisotopic Mass: 381.09 Da
• Topological Polar Surface Area: 46.900 Ų
• Heavy Atom Count: 27
• Formal Charge: 0
• Complexity: 513.000
• 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