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Details

Stereochemistry ACHIRAL
Molecular Formula C9H14Si
Molecular Weight 150.293
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENYLTRIMETHYLSILANE

SMILES

C[Si](C)(C)C1=CC=CC=C1

InChI

InChIKey=KXFSUVJPEQYUGN-UHFFFAOYSA-N
InChI=1S/C9H14Si/c1-10(2,3)9-7-5-4-6-8-9/h4-8H,1-3H3

HIDE SMILES / InChI

Molecular Formula C9H14Si
Molecular Weight 150.293
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Octa, deca, and dodeca(4-nitrophenyl) cage silsesquioxanes via 4-trimethylsilylphenyl derivatives.
2010-04-07
The beta effect of silicon in phenyl cations.
2007-12-26
Polymer supported naphthalene-catalysed sodium reactions.
2007-11-07
Large Raman-scattering activities for the low-frequency modes of substituted benzenes: induced polarizability and stereo-specific ring-substituent interactions.
2006-03-14
Trimethylsilylation of framework Brønsted acid sites in microporous zeolites and silico-aluminophosphates.
2003-11-19
Hydrosilylation of carbonyl compounds using a PhSeSiMe(3)/Bu(3)SnH/AIBN system.
2001-10-04
One-pot conversion of allyl alcohols into selenochroman derivatives.
2001-09
A novel type of nucleophilic substitution reactions on nonactivated aromatic compounds and benzene itself with trimethylsiliconide anions.
2001-04-19
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 22:47:40 GMT 2025
Edited
by admin
on Mon Mar 31 22:47:40 GMT 2025
Record UNII
PX1SG1Q5YP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-96828
Preferred Name English
PHENYLTRIMETHYLSILANE
Systematic Name English
BENZENE, (TRIMETHYLSILYL)-
Systematic Name English
(TRIMETHYLSILYL)BENZENE
Systematic Name English
SILANE, TRIMETHYLPHENYL-
Systematic Name English
TRIMETHYLPHENYLSILANE
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
212-192-5
Created by admin on Mon Mar 31 22:47:40 GMT 2025 , Edited by admin on Mon Mar 31 22:47:40 GMT 2025
PRIMARY
CAS
768-32-1
Created by admin on Mon Mar 31 22:47:40 GMT 2025 , Edited by admin on Mon Mar 31 22:47:40 GMT 2025
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FDA UNII
PX1SG1Q5YP
Created by admin on Mon Mar 31 22:47:40 GMT 2025 , Edited by admin on Mon Mar 31 22:47:40 GMT 2025
PRIMARY
NSC
96828
Created by admin on Mon Mar 31 22:47:40 GMT 2025 , Edited by admin on Mon Mar 31 22:47:40 GMT 2025
PRIMARY
PUBCHEM
69849
Created by admin on Mon Mar 31 22:47:40 GMT 2025 , Edited by admin on Mon Mar 31 22:47:40 GMT 2025
PRIMARY
EPA CompTox
DTXSID6061109
Created by admin on Mon Mar 31 22:47:40 GMT 2025 , Edited by admin on Mon Mar 31 22:47:40 GMT 2025
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