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Trichlorosilane

ALDRICH/175552 - 99%

CAS Number: 10025-78-2
Empirical Formula (Hill Notation): HCl3Si
Molecular Weight: 135.45
EC Number: 233-042-5
MDL Number: MFCD00011518
Linear Formula: SiHCl3
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-175552-5G 5 g
$52.90
1/EA
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45-175552-100G 100 g
$61.20
1/EA
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45-175552-500G 500 g
$159.00
1/EA
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assay 99%
bp 32-34 °C (lit.)
density 1.342 g/mL at 25 °C (lit.)
expl. lim. 70 %
form liquid
InChI 1S/Cl3HSi/c1-4(2)3/h4H
InChI key ZDHXKXAHOVTTAH-UHFFFAOYSA-N
Quality Level 200 
SMILES string Cl[SiH](Cl)Cl
storage temp. 2-8°C
vapor density 1 (vs air)
vapor pressure 9.75 psi ( 20 °C)
Application: Trichlorosilane has been used to synthesize 11-dicyclohexylphosphino-12-phenyl-9,10-dihydro-9,10-ethenoanthracene (H-KITPHOS) via reduction of 11-dicyclohexylphosphinoyl-12-phenyl-9,10-dihydro-9,10-ethenoanthracene.
Other possible applications:
• Asymmetric reduction of N-aryl ketimines in the presence of a novel

L-valine-derived catalyst to form secondary amines.
• Hydrosilylation of imidazolinones to form chiral imidazolidinones in the presence of a 2,2′-bispyrrolidine based Lewis base organocatalyst.
• Trichlorosilane activated with chiral N-formylproline

derivatives is an effective reagent for the reduction of imines to form
enantiomerically enriched amines.
• Trichlorosilane reacts with dimethylformamide to form hypervalent hydridosilicates, which can reduce aldehydes to alcohols, imines to amines, and also for the reductive amination of aldehydes.

General description: Trichlorosilane is generally used for the asymmetric hydrosilylation of olefins in the presence of palladium catalysts coordinated with chiral monodentate phosphorus ligands to generate chiral organosilanes.
Packaging: 5, 100, 250, 500 g in Sure/Seal™
Purity 99%
bp 32-34 °C (lit.)
Density 1.342 g/mL at 25 °C (lit.)
Storage Temp. 2-8°C
UNSPSC 12352101

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