Flusilazole - analytical standard, ≥98%, used for Flusilazole may be used as a reference standard for the determination of flusilazole in water samples using solid-phase extraction (SPE) method using multi-walled carbon nanotubes as adsorbent coupled with

CAS: 85509-19-9 Cat. No.: F109956 Summenformel: C₁₆H₁₅F₂N₃Si Molekulargewicht: 315.39 Beilstein Registry Number: 5824097 EG-Nummer: 617-717-5

GRADE & PURITY Analytical standard, ≥98%

Synonyms

DPX 6573 | NCGC00259035-01 | EPA Pesticide Chemical Code 128835 | Flusilazole [ISO] | Punch (pesticide) | Flusilazole 10 microg/mL in Acetonitrile | NCGC00164304-01 | CAS-85509-19-9 | UNII-F3WG2VVD87 | CHEBI:81922 | Olymp | DTXCID704235 | Flusilazol | Tri

Storage

Protected from light,Store at -20°C

Shipped In

Ice chest + Ice pads

Übersicht

Flusilazole is an organosilicon fungicide, which belongs to the class of sterol demethylation inhibitors. Its mode of action involves the inhibition of lanosterol 1,4-α-demethylation in fungal sterol biosynthesis.

Specifications

Synonyme

DPX 6573 | NCGC00259035-01 | EPA Pesticide Chemical Code 128835 | Flusilazole [ISO] | Punch (pesticide) | Flusilazole 10 microg/mL in Acetonitrile | NCGC00164304-01 | CAS-85509-19-9 | UNII-F3WG2VVD87 | CHEBI:81922 | Olymp | DTXCID704235 | Flusilazol | Tri

Spezifikationen & Reinheit

analytical standard, ≥98%

Anmeldung

Flusilazole may be used as a reference standard for the determination of flusilazole in water samples using solid-phase extraction (SPE) method using multi-walled carbon nanotubes as adsorbent coupled with high-performance liquid chromatography (HPLC).

Storage

Protected from light,Store at -20°C

Verschickt in

Ice chest + Ice pads

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

Note

Analytischer Standard

Reinheit

≥98%

Namen und Kennungen

Pubchem Sid

508813944

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508813944

Kanonisches Lächeln

C[Si](CN1C=NC=N1)(C2=CC=C(C=C2)F)C3=CC=C(C=C3)F

IUPAC Name

bis(4-fluorophenyl)-methyl-(1,2,4-triazol-1-ylmethyl)silane

InChIKey

FQKUGOMFVDPBIZ-UHFFFAOYSA-N

INCHI

1S/C16H15F2N3Si/c1-22(12-21-11-19-10-20-21,15-6-2-13(17)3-7-15)16-8-4-14(18)5-9-16/h2-11H,12H2,1H3

Isomere SMILES

C[Si](CN1C=NC=N1)(C2=CC=C(C=C2)F)C3=CC=C(C=C3)F

WGK Deutschland

3

RTECS

XZ4105000

Molekulargewicht

315.39

Beilstein

5824097

Reaxy-Rn

5824097

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5824097&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: Benzene and substituted derivatives
• Subclass: Halobenzenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Fluorobenzenes
• Alternative Parents: Alkylarylsilanes Aryl fluorides Triazoles Heteroaromatic compounds Organic metalloid salts Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organofluorides Hydrocarbon derivatives Alkylsilanes
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Fluorobenzene - Alkylarylsilane - Aryl fluoride - Aryl halide - Azole - Heteroaromatic compound - 1,2,4-triazole - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Alkylsilane - Organic nitrogen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Hydrocarbon derivative - Organopnictogen compound - Organosilicon compound - Organic salt - Aromatic heteromonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as fluorobenzenes. These are compounds containing one or more fluorine atoms attached to a benzene ring.
• External Descriptors: Conazole fungicides

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

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RXRA Tclin Retinoid X receptor alpha (3637 Activities)

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NR1H4 Tclin Bile acid receptor FXR (6228 Activities)

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Ppard Peroxisome proliferator-activated receptor delta (358 Activities)

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Oculimacula yallundae (312 Activities)

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Plenodomus lingam (178 Activities)

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Parastagonospora nodorum (325 Activities)

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Puccinia recondita (281 Activities)

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Cladosporium cucumerinum (320 Activities)

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Nr1i2 Nuclear receptor subfamily 1 group I member 2 (14 Activities)

Discover Target: Nr1i2

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Neofusicoccum australe (78 Activities)

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Plenodomus biglobosus (26 Activities)

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Diplodia mutila (102 Activities)

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Neofusicoccum luteum (172 Activities)

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Oculimacula acuformis (31 Activities)

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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Empfindlichkeit: Light sensitive.
• Schmelzpunkt (°C): 53-55°C
• Molekulargewicht: 315.390 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 315.1 Da
• Monoisotopic Mass: 315.1 Da
• Topological Polar Surface Area: 30.700 Ų
• Heavy Atom Count: 22
• Formal Charge: 0
• Complexity: 333.000
• 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

XLogP3