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Ethyne-1,2-diyldisilane, also known as 1,2-bis(trifluorosilyl)ethyne or 1,2-diethynyldisilane, is an organosilicon compound with the chemical formula (SiH3)2C2. It is a colorless, volatile liquid that is highly sensitive to air and moisture. ethyne-1,2-diyldisilane is characterized by a triple bond between two carbon atoms (C≡C) and two silicon atoms (Si) connected to the carbon atoms through single bonds. Ethyne-1,2-diyldisilane is an important precursor in the synthesis of various organosilicon compounds and materials, such as polymers, ceramics, and electronic devices. Due to its reactivity, it is typically handled under an inert atmosphere or in a vacuum to prevent unwanted side reactions.

1070-76-4

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1070-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1070-76-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1070-76:
(6*1)+(5*0)+(4*7)+(3*0)+(2*7)+(1*6)=54
54 % 10 = 4
So 1070-76-4 is a valid CAS Registry Number.

1070-76-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-silylethynylsilane

1.2 Other means of identification

Product number -
Other names ethynediyl-bis-silane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1070-76-4 SDS

1070-76-4Downstream Products

1070-76-4Relevant academic research and scientific papers

Silylenes of the elemental composition C2H4Si2: Generation and matrix-spectroscopic identification

Maier, Guenther,Reisenauer, Hans Peter,Meudt, Andreas

, p. 1291 - 1295 (2007/10/03)

Pulsed flash pyrolysis in combination with matrix isolation of three precursor molecules (10, 11, 12) led to the formation of silylsilacyclopropenylidene (1), which was identified by comparison of experimental and calculated (BLYP/6-31G*) IR spectra for both, unlabeled 1 and its perdeuterated isotopomer. Upon irradiation of matrix-isolated silylsilacyclopropenylidene (1) a second C2H4Si2 isomer, namely (silylethynyl)silylene (4) was formed. However, no evidence could be found for the formation of disilatetrahedrane or 1,2-or 1,3-disilacyclobutadiene.

Synthesis and Molecular Structure of Silylated Ethenes and Acetylenes

Ruedinger, Christoph,Beruda, Holger,Schmidbaur, Hubert

, p. 1348 - 1360 (2007/10/02)

Disilylacetylene (1) has been obtained from LiAlH4 reduction of bis(trichlorosilyl)acetylene (2) and bisacetylene (4).The catalytic hydrosilylation of 2 with HSiCl3 affords tris(trichlorosilyl)ethene (5) and 1,1,2-tris(trichlorosilyl)ethane (6).The synthesis of 6, trans-bis(trichlorosilyl)ethene (8) and 1,1-bis(trichlorosilyl)ethene (9) has been accomplished by hydrosilylation of trichlorosilylacetylene (7) which was synthesized by the reaction of trichloro(trifluoromethylsulfonyloxy)silane with sodium acetylide.Reductive elimination of halogen from 1,1,1,2-tetrachloro-bis(trichlorosilyl)ethane (10) and 1,2-dibromo-1,1-bis(trichlorosilyl)ethane (13) gave the corresponding ethenes 1,1-dichloro-bis-(trichlorosilyl)ethene (11), trichloro-trichlorosilylethene (12), 1,1-bis(trichlorosilyl)ethene (9) and 1-chloro-2,2-bis(trichlorosilyl)ethene (14).Tetrakis(trichlorosilyl)ethene (15) has been obtained in a three step synthesis starting from chloromethyl-trichlorosilane or dichloromethyl-trichlorosilane.By LiAlH4 reduction of trichlorosilylethenes under various reaction conditions, the silylethenes trans-dichloro-di(silyl)ethene (16), 1,1-dichloro-di(silyl)ethene (17), trichloro-silylethene (18), 1-bromo-1-silylethene (19), trans-di(silyl)ethene (20), 1-chloro-2,2-di(silyl)ethene (21), tri(silyl)ethene (22), and 1,1,2-tri(silyl)ethane (23) could be generated.Silylethyne and silyl-chloroethyne were identified as side products.The crystal and molecular structures of 2, 5 and 15 have been determined by single crystal X-ray diffraction. 2 and 5 crystallize from the melt in the monoclinic space groups Cc and P21/n, respectively. 15 has been crystallized by sublimation (orthorhombic, space group Pbca). 5 and 15 feature strongly distorted ethene skeletons with a double bond twist of 28.1 deg in 15. - Keywords: Silanes, Trichlorosilanes, Polysilylethenes, Carbon Halogenated Silylolefines

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