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18586-22-6

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  • 1,5-DIVINYL-3,3-DIPHENYL-1,1,5,5-TETRA-METHYLTRISILOXANE

    Cas No: 18586-22-6

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18586-22-6 Usage

General Description

1,5-Divinyl-3,3-diphenyl-1,1,5,5-tetramethyltrisiloxane is a chemical compound with the molecular formula C28H34O2Si3. It belongs to the class of organosilicon compounds and is commonly used as a crosslinking agent in the production of silicones. This chemical has three silicon atoms bonded to oxygen atoms, and its structure includes phenyl and vinyl groups. It is also used in the manufacture of sealants, adhesives, and coatings, where its unique properties contribute to the strength, flexibility, and thermal stability of the final product. Additionally, it is utilized in the electronics industry for encapsulation and potting of electronic components. Overall, 1,5-divinyl-3,3-diphenyl-1,1,5,5-tetramethyltrisiloxane plays an important role in various industrial applications due to its versatile and valuable properties.

Check Digit Verification of cas no

The CAS Registry Mumber 18586-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,8 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18586-22:
(7*1)+(6*8)+(5*5)+(4*8)+(3*6)+(2*2)+(1*2)=136
136 % 10 = 6
So 18586-22-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H28O2Si3/c1-7-23(3,4)21-25(22-24(5,6)8-2,19-15-11-9-12-16-19)20-17-13-10-14-18-20/h7-18H,1-2H2,3-6H3

18586-22-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name bis[[ethenyl(dimethyl)silyl]oxy]-diphenylsilane

1.2 Other means of identification

Product number -
Other names 1,1,5,5-Tetramethyl-3,3-diphenyl-1,5-divinyltrisiloxane

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:18586-22-6 SDS

18586-22-6Downstream Products

18586-22-6Relevant articles and documents

Preparation method of 1,5-divinyl-3,3-diphenyl-1,1,5,5-tetramethyltrisiloxane

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Paragraph 0063-0065, (2019/09/14)

The invention relates to a preparation method of 1,5-divinyl-3,3-diphenyl-1,1,5,5-tetramethyltrisiloxane. The preparation method comprises the steps: under the protection of protective gas, mixing anorganic solvent, diphenylsilyl glycol, divinyltetramethyldisiloxane and a catalyst at a ratio, raising the temperature for reflux, performing a reaction, performing reflux and separation on water generated during the reaction by using a water separator, lowering the temperature after completion of the reaction, performing neutralization and washing with water so as to obtain an organic phase, andperforming vacuum distillation so as to obtain the product. The problems of environmental protection and low selectivity which are caused by using chlorosilane as a reaction raw material are solved, and the preparation method has the advantages of simple operation, a high catalytic efficiency, a high yield, good safety and the like.

Method of manufacturing polyimidesiloxane compd. divinylbenzyl

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Paragraph 0021; 0023-0025, (2018/02/06)

PROBLEM TO BE SOLVED: To provide a production method by which a divinyl siloxane compound such as a divinyltrisiloxane is obtained in a high yield without using dimethyl vinyl chlorosilane.SOLUTION: A method of producing a divinyl siloxane compound represented by general formula (3) includes reacting of a silane diol compound with a divinyl siloxane compound by using an alkali metal catalyst. In the general formula(3), Ris an aryl group having 6 to 10 carbon atoms, Ris an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, a cycloalkyl group or a cycloalkenyl group having 5 to 10 carbon atoms, an aryl group having 6 to 10 carbon atoms, or an aralkyl group having 7 to 10 carbon atoms, and Rand Rare each independently an alkyl group having 1 to 4 carbon atoms.

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