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Silane, (1-phenyl-1,2-ethanediyl)bis[trichloro-], also known as bis(1-phenyl-1,2-ethanediyl)trichlorosilane, is a chemical compound with the formula (C6H4CH2CH2)2SiCl3. It is a colorless to pale yellow liquid that is sensitive to air and moisture. This organosilicon compound is used as a coupling agent in the production of composite materials, particularly in the reinforcement of rubber and plastics with fillers. It enhances the adhesion between the organic matrix and inorganic fillers, improving the mechanical properties of the composite. The compound is also utilized in the synthesis of other organosilicon compounds and as a cross-linking agent in the production of silicone resins. Due to its reactivity with moisture, it is typically handled under an inert atmosphere and is considered hazardous, requiring proper safety measures during storage and use.

3401-10-3

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3401-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3401-10-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,0 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3401-10:
(6*3)+(5*4)+(4*0)+(3*1)+(2*1)+(1*0)=43
43 % 10 = 3
So 3401-10-3 is a valid CAS Registry Number.

3401-10-3SDS

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 trichloro-(1-phenyl-2-trichlorosilylethyl)silane

1.2 Other means of identification

Product number -
Other names 1.2-Bis-trichlorsilyl-2-phenyl-ethan

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:3401-10-3 SDS

3401-10-3Relevant academic research and scientific papers

Trichlorosilyl groups containing organochlorosilanes and their preparation methods by the double-silylation of olefins with trichlorosilane

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Page 3, (2008/06/13)

The present invention provides organosilicon compounds containing two trichlorosilyl groups and their preparation methods. Organosilicon compounds of formula II are prepared by reacting linear chain or cyclic olefins of formula I with trichlorosilane in the presence of quaternary organophosphonium salt as a catalyst.R1—HC=CH—R2??(I) 1In formulas I and II, R1 and R2 may be identical or different and represent a hydrogen atom, a linear or a cyclic C1-C8 alkyl, a linear or a cyclic C1-C8 alkenyl, benzyl, phenyl, a C1-C8 alkyl substituted phenyl group, two functional groups between R1 and R2 may be covalently bonded to form a C4-C8 ring with or without a carbon-carbon double bond.

Asymmetric synthesis of 1-aryl-1,2-ethanediols from arylacetylenes by palladium-catalyzed asymmetric hydrosilylation as a key step

Shimada, Toyoshi,Mukaide, Kotaro,Shinohara, Akihiro,Han, Jin Wook,Hayashi, Tamio

, p. 1584 - 1585 (2007/10/03)

Double hydrosilylation of arylacetylenes with trichlorosilane catalyzed first by platinum and second by a chiral monophosphine-palladium complex generated the corresponding 1,2-bis(silyl)-1-arylethanes, the oxidation of which with hydrogen peroxide gave 1-aryl-1,2-diols of high enantiomeric purity (94-98% ee) in high yields. Copyright

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