DIISOPROPYLDICHLOROSILANE
DIISOPROPYLDICHLOROSILANE Basic information
- Product Name:
- DIISOPROPYLDICHLOROSILANE
- Synonyms:
-
- dichlorodiisopropylisilane
- DIISOPROPYLDICHLOROSILANE
- DICHLORODIISOPROPYLSILANE
- DICHLORODIISOPROPYSILANE
- Silane, dichlorobis(1-methylethyl)-
- Dichlorodiisopropylsilane >=97.0% (GC)
- dichloro-di(propan-2-yl)silane
- Diisopropyldichlorosilane, 97%, for synthesis
- CAS:
- 7751-38-4
- MF:
- C6H14Cl2Si
- MW:
- 185.17
- Product Categories:
-
- Dichlorosilanes
- Dichlorosilanes (for Polysilanes)
- Functional Materials
- Reagent for High-Performance Polymer Research
- Si (Classes of Silicon Compounds)
- Si-Cl Compounds
- Mol File:
- 7751-38-4.mol
DIISOPROPYLDICHLOROSILANE Chemical Properties
- Melting point:
- <0°C
- Boiling point:
- 66 °C27 mm Hg(lit.)
- Density
- 1.026 g/mL at 20 °C(lit.)
- refractive index
- n20/D 1.444
- Flash point:
- 43°C
- solubility
- sol most organic solvents.
- form
- clear liquid
- Specific Gravity
- 1.026
- color
- Colorless to Light yellow to Light orange
- Hydrolytic Sensitivity
- 8: reacts rapidly with moisture, water, protic solvents
- BRN
- 1736244
- CAS DataBase Reference
- 7751-38-4(CAS DataBase Reference)
Safety Information
- Hazard Codes
- C
- Risk Statements
- 10-34
- Safety Statements
- 28-36/37/39-45
- RIDADR
- UN 2986 8/PG 2
- WGK Germany
- 3
- F
- 10-21
- TSCA
- No
- HazardClass
- 3/8
- PackingGroup
- II
- HS Code
- 29319090
MSDS
- Language:English Provider:SigmaAldrich
DIISOPROPYLDICHLOROSILANE Usage And Synthesis
Physical properties
bp 50–55°C/5 mmHg.
Uses
Dichlorodiisopropylsilane can be used in nucleoside 3',5'-hydroxy protection; component in Peterson alkenation reaction.
The use of silicon groups as protection for hydroxy groups has been widely exploited.3 One potentially useful way to protect a nucleoside is by using a protecting group which spans the 3- and 5-hydroxy groups. One of the useful groups which can be used as a bifunctional protecting group in nucleosides is the diisopropylsilyl group. Reaction of the nucleoside with dichlorodiisopropylsilane and imidazole in DMF gives the protected nucleoside (eq 1).This method has not been widely used; the more common 3',5'-hydroxy-bridging protecting group is a tetraisopropyldisiloxy group.
Preparation
conveniently prepared by the reaction of diisopropylsilane in carbon tetrachloride with palladium(II) chloride at 140°C for 8 h in a steel bomb.Washing the residue with ether and removing the ether by rotary evaporation yields the product which is purified by distillation to yield a clear colorless oil.
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DIISOPROPYLDICHLOROSILANE(7751-38-4)Related Product Information
- DIMESITYLDICHLOROSILANE
- Dichloromethylvinylsilane
- DIISOPROPYLETHOXYSILANE
- Chlorodimethylsilane
- Dimethyldimethoxysilane
- DICHLOROISOBUTYLMETHYLSILANE
- DIISOBUTYLCHLOROSILANE
- DIISOBUTYLDIETHOXYSILANE
- Diisobutyldimethoxysilane
- 3,6-BIS(TERT-BUTYL)CARBAZOLE
- DICYCLOHEXYLDICHLOROSILANE
- DI-TERT-BUTYLDICHLOROSILANE
- DIISOPROPYLCHLOROSILANE
- Dichlorodiethylsilane
- DIISOPROPYLDICHLOROSILANE
- DIISOPROPYLSILANE
- ISOPROPYLMETHYLDICHLOROSILANE
- Dicyclopentyldichlorosilane