Fluorotriphenylsilane - ≥97%(GC) , CAS No.379-50-0

CAS: 379-50-0 Cat. No.: F140889 Peso molecular: 278.4 Beilstein Registry Number: 2941368 Número EC: 206-832-2

GRADE & PURITY ≥97%(GC)

Synonyms

Fluorotriphenylsilane | SCHEMBL701465 | EN300-304297 | Triphenylfluorosilane | 1,1',1''-(Fluorosilylidyne)tris[benzene] | FS-5450 | NSC43086 | UBGXLEFOIVWVRP-UHFFFAOYSA- | Triphenylsilyl fluoride | Silane, fluorotriphenyl- | C18H15FSi | MFCD00017899 | UNI

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

A useful derivatization agent.

Specifications

Sinónimos

Fluorotriphenylsilane | SCHEMBL701465 | EN300-304297 | Triphenylfluorosilane | 1, 1', 1''-(Fluorosilylidyne)tris[benzene] | FS-5450 | NSC43086 | UBGXLEFOIVWVRP-UHFFFAOYSA- | Triphenylsilyl fluoride | Silane, fluorotriphenyl- | C18H15FSi | MFCD00017899 | UNI

Especificaciones y pureza

≥97%(GC)

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥97%(GC)

Nombres e identificadores

• Sonrisas canónicas: C1=CC=C(C=C1)[Si](C2=CC=CC=C2)(C3=CC=CC=C3)F
• IUPAC Name: fluoro(triphenyl)silane
• InChIKey: UBGXLEFOIVWVRP-UHFFFAOYSA-N
• INCHI: 1S/C18H15FSi/c19-20(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
• Isómeros SMILES: C1=CC=C(C=C1)[Si](C2=CC=CC=C2)(C3=CC=CC=C3)F
• WGK Alemania: 3
• Peso molecular: 278.4
• Beilstein: 2941368
• Reaxy-Rn: 2941368
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2941368&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzene and substituted derivatives
• Alternative Parents: Silyl monohalides Organoheterosilanes Organic metalloid salts Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Monocyclic benzene moiety - Silyl monohalide - Organoheterosilane - Organic metalloid salt - Hydrocarbon derivative - Organic salt - Organosilicon compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
• External Descriptors: Not available

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

Propiedades químicas y físicas

• Sensibilidad: Air sensitive.
• Punto de ebullición (°C): 210°C
• Punto de fusión (°C): 62-64°C
• Peso molecular: 278.400 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 278.093 Da
• Monoisotopic Mass: 278.093 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 20
• Formal Charge: 0
• Complexity: 240.000
• 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

Referencias

1. Xiaogang Guo, Taotao Liang.  (2019)  Super-Efficient Synthesis of Mesh-like Superhydrophobic Nano-Aluminum/Iron (III) Oxide Energetic Films.  Materials,  12  (2): (234).  [PMID:30641952] [10.3390/ma12020234]