175552
Trichlorosilane
99%
Synonym(s):
Hydrotrichlorosilane, Silicochloroform, Silicon chloride hydride, Trichloromonosilane
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
SiHCl3
CAS Number:
Molecular Weight:
135.45
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352101
EC Number:
233-042-5
MDL number:
Assay:
99%
Form:
liquid
vapor density
1 (vs air)
Quality Level
vapor pressure
9.75 psi ( 20 °C)
assay
99%
form
liquid
expl. lim.
70 %
bp
32-34 °C (lit.)
density
1.342 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
Cl[SiH](Cl)Cl
InChI
1S/Cl3HSi/c1-4(2)3/h4H
InChI key
ZDHXKXAHOVTTAH-UHFFFAOYSA-N
General description
Trichlorosilane is used as a reducing agent in certain chemical reactions or as a starting material for the synthesis of various organosilicon compounds. 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.
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:
L-valine-derived catalyst to form secondary amines.
derivatives is an effective reagent for the reduction of imines to form
enantiomerically enriched amines.
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.
signalword
Danger
hcodes
supp_hazards
Storage Class
4.3 - Hazardous materials which set free flammable gases upon contact with water
wgk
WGK 1
flash_point_f
<-2.2 °F - Equilibrium method
flash_point_c
< -19 °C - Equilibrium method
ppe
Faceshields, Gloves, Goggles
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 1 - Skin Corr. 1A - Water-react. 1
Regulatory Information
监管及禁止进口产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Amira Namsi et al.
Molecules (Basel, Switzerland), 24(18) (2019-09-14)
Neurodegenerative diseases are characterized by oxidative stress, mitochondrial damage, and death of neuronal cells. To counteract such damage and to favor neurogenesis, neurotrophic factors could be used as therapeutic agents. Octadecaneuropeptide (ODN), produced by astrocytes, is a potent neuroprotective agent.
Trichlorosilane-dimethylformamide (Cl3SiH-DMF) as an efficient reducing agent. Reduction of aldehydes and imines and reductive amination of aldehydes under mild conditions using hypervalent hydridosilicates
Kobayashi S
Chemistry Letters (Jpn), 25(5), 407-408 (1996)
Guiding the self-assembly of a second-generation polyphenylene dendrimer into well-defined patterns.
An J J Ver Heyen et al.
Small (Weinheim an der Bergstrasse, Germany), 4(8), 1160-1167 (2008-07-25)
A second-generation polyphenylene dendrimer 1 is shown to self-assemble into nanofibers. To guide the formation of the dendrimer fibers into well-defined patterns, 1H,1H,2H,2H-perfluorodecyltrichlorosilane is grafted in the gas phase onto a silicon substrate. De-wetting of the solution on the nanopatterned
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 175552-100G | 04061838752345 |
| 175552-PZ | 04061823777407 |
| 175552-5G | 04061837789564 |
| 175552-500G | 04061838752352 |
| 175552-250G | 04061837789557 |