80-10-4 Usage
Description
Dichlorodiphenylsilane, also known as Diphenyldichlorosilane, is a colorless liquid with a pungent odor. It is a silane-based surface modifier and a precursor used in the synthesis of silica-based materials. Its chemical properties include being corrosive to metals and tissue, and it can burn, although it may require some effort to ignite. When decomposed by water, it forms hydrochloric acid with the evolution of heat.
Uses
Used in Surface Modification Industry:
Dichlorodiphenylsilane is used as a surface modifier to provide toughness, durability, and resistance to shock. It enhances the surface properties of materials, making them more robust and resistant to various environmental factors.
Used in Synthesis of Silica-based Materials:
Dichlorodiphenylsilane serves as a precursor in the synthesis of silica-based materials, which have a wide range of applications in various industries due to their unique properties.
Used in Organic Light Emitting Diodes (OLEDs) Industry:
Dichlorodiphenylsilane is used in the synthesis of a host material for the fabrication of blue phosphorescent OLEDs. This application takes advantage of its ability to contribute to the development of advanced display technologies with improved performance and energy efficiency.
Reactivity Profile
Chlorosilanes, such as Dichlorodiphenylsilane, are compounds in which silicon is bonded to from one to four chlorine atoms with other bonds to hydrogen and/or alkyl groups. Chlorosilanes react with water, moist air, or steam to produce heat and toxic, corrosive fumes of hydrogen chloride. They may also produce flammable gaseous H2. They can serve as chlorination agents. Chlorosilanes react vigorously with both organic and inorganic acids and with bases to generate toxic or flammable gases.
Flammability and Explosibility
Notclassified
Safety Profile
A poison irritant to
skin, eyes, and mucous membranes. See also
CHLOROSILANES. Can react vigorously
with oxidizing materials. When heated to
decomposition or on contact with acid or
acid fumes it emits toxic fumes of Cl-.
Check Digit Verification of cas no
The CAS Registry Mumber 80-10-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80-10:
(4*8)+(3*0)+(2*1)+(1*0)=34
34 % 10 = 4
So 80-10-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H10.Cl2H2Si/c1-3-7-11(8-4-1)12-9-5-2-6-10-12;1-3-2/h1-10H;3H2
80-10-4Relevant articles and documents
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Rochow,Gilliam
, p. 1772 (1945)
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Neutral-Eosin-Y-Photocatalyzed Silane Chlorination Using Dichloromethane
Fan, Xuanzi,Xiao, Pin,Jiao, Zeqing,Yang, Tingting,Dai, Xiaojuan,Xu, Wengang,Tan, Jin Da,Cui, Ganglong,Su, Hongmei,Fang, Weihai,Wu, Jie
, p. 12580 - 12584 (2019/08/16)
Chlorosilanes are versatile reagents in organic synthesis and material science. A mild pathway is now reported for the quantitative conversion of hydrosilanes to silyl chlorides under visible-light irradiation using neutral eosin Y as a hydrogen-atom-transfer photocatalyst and dichloromethane as a chlorinating agent. Stepwise chlorination of di- and trihydrosilanes was achieved in a highly selective fashion assisted by continuous-flow micro-tubing reactors. The ability to access silyl radicals using photocatalytic Si?H activation promoted by eosin Y offers new perspectives for the synthesis of valuable silicon reagents in a convenient and green manner.
Electrochemical properties of arylsilanes
Biedermann, Judith,Wilkening, H. Martin R.,Uhlig, Frank,Hanzu, Ilie
, p. 13 - 18 (2019/03/27)
In the past, the electrochemical properties of organosilicon compounds were investigated for both fundamental reasons and synthesis purposes. Little is, however, known about the electrochemical behaviour of hydrogen-bearing arylsilanes. Here, we throw light on the electrochemical properties of 11 arylsilanes compounds, 2 of them synthesized for the first time. The oxidation potentials are found to depend on both the nature and number of the aryl groups. Based on these findings it was possible to establish some variation trends that match the expected structure–property correlations. Furthermore, we present first insights into the electrochemical reaction kinetics behind and identify several soluble electrochemical oxidation products.