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DIISOPROPYLDICHLOROSILANE

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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
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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)
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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
10-21
TSCA 
No
HazardClass 
3/8
PackingGroup 
II
HS Code 
29319090

MSDS

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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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