Chlorotriphenylsilane - ≥95% , CAS No.76-86-8

CAS: 76-86-8 Cat. No.: C103643 Formule: C₁₈H₁₅ClSi Poids moléculaire: 294.85 Beilstein Registry Number: 1820487 Numéro CE: 200-989-0

GRADE & PURITY ≥95%

Synonyms

TPSCl | EN300-226986 | NSC 102804 | Triphenylchlorosilane | Triphenylsilyl chloride | SILANE, CHLOROTRIPHENYL- | T0939 | AI3-51278 | DTXSID70870398 | Chlorotriphenylsilane | triphenylsilylchloride | A838876 | MNKYQPOFRKPUAE-UHFFFAOYSA- | Triphenylsilicon

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice,FedEx DG Service

Vue d’ensemble

Chlorotriphenylsilane is used as a silylating agent. It is also used as a pharmaceutical intermediate.

Specifications

Synonymes

TPSCl | EN300-226986 | NSC 102804 | Triphenylchlorosilane | Triphenylsilyl chloride | SILANE, CHLOROTRIPHENYL- | T0939 | AI3-51278 | DTXSID70870398 | Chlorotriphenylsilane | triphenylsilylchloride | A838876 | MNKYQPOFRKPUAE-UHFFFAOYSA- | Triphenylsilicon

Spécifications et pureté

≥95%

Conditions de stockage de stockage

Store at 2-8°C,Argon charged

Expédié en

Wet ice,FedEx DG Service

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Pureté

≥95%

Noms et identifiants

• Pubchem Sid: 508811636
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/508811636
• Sourires canoniques: C1=CC=C(C=C1)[Si](C2=CC=CC=C2)(C3=CC=CC=C3)Cl
• IUPAC Name: chloro(triphenyl)silane
• InChIKey: MNKYQPOFRKPUAE-UHFFFAOYSA-N
• INCHI: 1S/C18H15ClSi/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
• Isomères SMILES: C1=CC=C(C=C1)[Si](C2=CC=CC=C2)(C3=CC=CC=C3)Cl
• WGK Allemagne: 3
• RTECS: VV2720000
• Numéro ONU: 3261
• Groupe d'emballage: II
• Poids moléculaire: 294.85
• Beilstein: 1820487
• Reaxy-Rn: 1820487
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1820487&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzene and substituted derivatives
• Alternative Parents: Silyl monohalides Organochlorosilanes Organic metalloid salts Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Monocyclic benzene moiety - Silyl monohalide - Organoheterosilane - Organochlorosilane - Organic metalloid salt - Hydrocarbon derivative - Organic salt - Organosilicon compound - Aromatic homomonocyclic compound
• Description: 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

Propriétés chimiques et physiques

• Solubilité: Reacts with water.
• Sensibilité: Moisture & heat & light sensitive
• Point d'ébullition (°C): 378°C
• Point de fusion (°C): 92-94°C
• Poids moléculaire: 294.800 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 3
• Exact Mass: 294.063 Da
• Monoisotopic Mass: 294.063 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

Références

1. Peng Liu, Yining Gao, Fazhou Wang, Lu Yang.  (2018)  Preparation of pervious concrete with 3-thiocyanatopropyltriethoxysilane modified fly ash and its use in Cd (II) sequestration.  Journal of Cleaner Production,      [PMID:] [10.1016/j.jclepro.2018.11.242]