tert -butyl (trichloro) silane

Structural formula
General
Surname	tert -butyl (trichloro) silane
other names	tert -butyltrichlorosilane
Molecular formula	C 4 H 9 Cl 3 Si
Brief description	white solid
External identifiers / databases
EC number	242-059-7
ECHA InfoCard	100.038.221
PubChem	87494
Wikidata	Q25385543
properties
Molar mass	191.56 g mol −1
Physical state	firmly
density	1.18 g cm −3
Melting point	97-100 ° C
boiling point	132-134 ° C
solubility	decomposes in water with violent reaction
safety instructions
H and P phrases	H: 228-314
	EUH: 014
	P: 210-280-305 + 351 + 338-310
	As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

tert -Butyl (trichlor) silane is a chemical compound from the group of organosilicon compounds .

Extraction and presentation

tert -Butyl (trichlor) silane can be obtained by reacting silicon tetrachloride with tert -butyllithium .

properties

tert -Butyl (trichlor) silane is a white crystalline flammable solid that decomposes violently in water. Your aqueous solution reacts strongly acidic.

use

tert -Butyl (trichlor) silane is used as an intermediate in the manufacture of other chemical compounds.

safety instructions

The vapors of tert- butyl (trichlor) silane can form an explosive mixture with air ( flash point 40 ° C).

Individual evidence

↑ ^a ^b ^c ^d ^e ^f ^g ^h ⁱ Entry for CAS no. 18171-74-9 in the GESTIS substance database of the IFA , accessed on May 1, 2016(JavaScript required) .
^ Carl L. Yaws: The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals Physical Properties for More Than 54,000 Organic and Inorganic Chemical Compounds, Coverage for C1 to C100 Organics and Ac to Zr Inorganics . Gulf Professional Publishing, 2015, ISBN 978-0-12-801146-1 , pp. 55 ( limited preview in Google Book search).
^ I. Fleming: Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 4 Compounds of Groups 15 (As, Sb, Bi) and Silicon Compounds . Georg Thieme Verlag, 2014, ISBN 3-13-171741-6 , p. 258 ( limited preview in Google Book search).
↑ Advances in Organometallic Chemistry . Academic Press, 1995, ISBN 978-0-12-031137-8 , pp. 16 ( limited preview in Google Book search).

[GESTIS-1] ↑ ^a ^b ^c ^d ^e ^f ^g ^h ⁱ Entry for CAS no. 18171-74-9 in the GESTIS substance database of the IFA , accessed on May 1, 2016(JavaScript required) .

[Carl_L._Yaws-2] Carl L. Yaws: The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals Physical Properties for More Than 54,000 Organic and Inorganic Chemical Compounds, Coverage for C1 to C100 Organics and Ac to Zr Inorganics . Gulf Professional Publishing, 2015, ISBN 978-0-12-801146-1 , pp. 55 ( limited preview in Google Book search).

[I._Fleming-3] I. Fleming: Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 4 Compounds of Groups 15 (As, Sb, Bi) and Silicon Compounds . Georg Thieme Verlag, 2014, ISBN 3-13-171741-6 , p. 258 ( limited preview in Google Book search).

[4] Advances in Organometallic Chemistry . Academic Press, 1995, ISBN 978-0-12-031137-8 , pp. 16 ( limited preview in Google Book search).