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
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
| 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
| Title | Date | PubMed |
|---|---|---|
| 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
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:47:40 GMT 2025
by
admin
on
Mon Mar 31 22:47:40 GMT 2025
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| Record UNII |
PX1SG1Q5YP
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| Record Status |
Validated (UNII)
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| Record Version |
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212-192-5
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768-32-1
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PX1SG1Q5YP
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96828
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69849
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DTXSID6061109
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