Home > Compound List > Product Information
Triphenylsilane_Molecular_structure_CAS_789-25-3)
Click picture or here to close

Triphenylsilane

Catalog No. 93130 Name Sigma Aldrich
CAS Number 789-25-3 Website http://www.sigmaaldrich.com
M. F. C18H16Si Telephone 1-800-521-8956
M. W. 260.40514 Fax
Purity ≥97.0% (GC) Email
Storage Chembase ID: 111500

SYNONYMS

Title
三苯基硅烷
IUPAC name
triphenylsilane
IUPAC Traditional name
triphenylsilane
Synonyms
1,1′,1′′-Silylidynetrisbenzene
Triphenylhydrosilane
NSC 12565

DATABASE IDS

CAS Number 789-25-3
Beilstein Number 978182
EC Number 212-333-0
MDL Number MFCD00003003
PubChem SID 24889803

PROPERTIES

Grade purum
Linear Formula (C6H5)3SiH
Purity ≥97.0% (GC)
Boiling Point 152 °C/2 mmHg(lit.)
Flash Point 76 °C
Flash Point 168.8 °F
Melting Point 43-45 °C(lit.)
Melting Point 43-45 °C
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26
German water hazard class 3

DETAILS

Description (English)
Other Notes
Silylating agent8
Application
Reactant or reagent:
• For catalytic hydrogen deuterium exchange reactions of silanes1
• To be oxidized by carbon nanotube-gold nanohybrids2
• For hydrolysis by ruthenium complexes3
• For hydrosilylation to produce enolsilanes4
• For synthesis of bromosilanes5
• For ozone oxidation of silyl-alkenes for synthesis of α-O-silylated acyloin derivatives6
• Used to synthesize hydrido silyl and bis(silyl) bis(imidazolinylidene) nickel complexes7
Description (简体中文)
Other Notes
硅烷化试剂8
Application
Reactant or reagent:
• For catalytic hydrogen deuterium exchange reactions of silanes1
• To be oxidized by carbon nanotube-gold nanohybrids2
• For hydrolysis by ruthenium complexes3
• For hydrosilylation to produce enolsilanes4
• For synthesis of bromosilanes5
• For ozone oxidation of silyl-alkenes for synthesis of α-O-silylated acyloin derivatives6
• Used to synthesize hydrido silyl and bis(silyl) bis(imidazolinylidene) nickel complexes7

REFERENCES