Triphenylsilane - ≥96%(GC) , CAS No.789-25-3

CAS: 789-25-3 Cat. No.: T162508 Peso molecular: 260.41 Beilstein Registry Number: 978182 Número EC: 212-333-0 PubChem CID: 6327682

GRADE & PURITY ≥96%(GC)

Synonyms

NSC 12565 | 1,1',1''-Silylidynetrisbenzene | UNII-UQL9QY2CS8 | Benzene, 1,1',1''-silylidynetris- | J-525126 | EN300-7425612 | T0661 | triphenylhydrosilane | triphenylsilicon;Triphenylsilane | S20600 | DTXSID10883583 | FT-0632957 | triphenylsilicon | AS-14

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

Reactant or reagent: . For catalytic hydrogen deuterium exchange reactions of silanes . To be oxidized by carbon nanotube-gold nanohybrids . For hydrolysis by ruthenium complexes . For hydrosilylation to produce enolsilanes . For synthesis of bromosilanes . For ozone oxidation of silyl-alkenes for synthesis of α-O-silylated acyloin derivatives . Used to synthesize hydrido silyl and bis(silyl) bis(imidazolinylidene) nickel complexes

Specifications

Sinónimos

NSC 12565 | 1, 1', 1''-Silylidynetrisbenzene | UNII-UQL9QY2CS8 | Benzene, 1, 1', 1''-silylidynetris- | J-525126 | EN300-7425612 | T0661 | triphenylhydrosilane | triphenylsilicon;Triphenylsilane | S20600 | DTXSID10883583 | FT-0632957 | triphenylsilicon | AS-14

Especificaciones y pureza

≥96%(GC)

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥96%(GC)

Nombres e identificadores

• Pubchem Sid: 504764065
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504764065
• Sonrisas canónicas: C1=CC=C(C=C1)[Si](C2=CC=CC=C2)C3=CC=CC=C3
• InChIKey: BZLZKLMROPIZSR-UHFFFAOYSA-N
• INCHI: 1S/C18H15Si/c1-4-10-16(11-5-1)19(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
• WGK Alemania: 1
• PubChem CID: 6327682
• Peso molecular: 260.41
• Beilstein: 978182
• Reaxy-Rn: 978182

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: Organosilicon compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Monocyclic benzene moiety - Hydrocarbon derivative - 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

• Solubilidad: Soluble in methanol. Decomposes in water
• Sensibilidad: Moisture sensitive;Air sensitive
• Punto de inflamación (°F): 168.8 °F
• Punto de inflamación (°C): 76 °C
• Punto de ebullición (°C): 152 °C/2 mmHg
• Punto de fusión (°C): 43-45 °C
• Peso molecular: 259.399 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 3
• Exact Mass: 259.094 Da
• Monoisotopic Mass: 259.094 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 202.000
• 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. Xue-Li Liu, Yi-Fan Chen, Yi-Wen Chen, Wei-Kang Peng, Han-Chun Liu.  (2022)  Preparation of carbosilane quaternary ammonium surfactants and surface activity.  TENSIDE SURFACTANTS DETERGENTS,  59  (5): (424-432).  [PMID:] [10.1515/tsd-2022-2428]

2. Jun Zhang, Kaijun Dong, Weimin Luo.  (2019)  PdCl2-catalyzed hydrodeoxygenation of 5-hydroxymethylfurfural into 2,5-dimethylfuran at room-temperature using polymethylhydrosiloxane as the hydrogen donor.  CHEMICAL ENGINEERING SCIENCE,      [PMID:] [10.1016/j.ces.2019.03.011]

3. Jing Neng, Chen Xiang, Kan Jia, Xiaohua Nie, Peilong Sun.  (2019)  Morphology-Controlled Versatile One-Pot Synthesis of Hydrophobic Gold Nanodots, Nanobars, Nanorods, and Nanowires and Their Applications in Surface-Enhanced Raman Spectroscopy.  Applied Sciences-Basel,  9  (5): (935).  [PMID:] [10.3390/app9050935]

4. Li Jingpeng, Zhang Meiyu, Li Wenxuan, Li Zhongshu, Zhu Tingshun, Yang Zhenyu.  (2025)  Direct dehydrocoupling facilitates efficient thiophene anchoring on silicon surfaces.  Nature Communications,  16  (1): (1-10).  [PMID:40683880] [10.1038/s41467-025-62002-7]