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7351-61-3

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7351-61-3 Usage

Description

(3-Methacryloyloxypropyl)trichlorosilane is a versatile and reactive chemical compound that serves as a coupling agent and adhesion promoter in various applications, particularly in the field of polymer and surface modification. It features a methacrylate functional group and a trichlorosilane group, which enable it to improve the adhesion between organic polymers and inorganic substrates, such as glass, metal, and ceramics. Additionally, it can be used as a surface modifier to enhance the hydrophobicity of materials. Due to its reactivity and functional groups, (3-Methacryloyloxypropyl)trichlorosilane is widely used in the production of adhesives, sealants, and coatings in various industrial applications.

Uses

Used in Adhesives and Sealants Industry:
(3-Methacryloyloxypropyl)trichlorosilane is used as a coupling agent and adhesion promoter for improving the bond strength between organic polymers and inorganic substrates, such as glass, metal, and ceramics. This enhances the performance and durability of adhesives and sealants in various applications.
Used in Coatings Industry:
(3-Methacryloyloxypropyl)trichlorosilane is used as a surface modifier to enhance the hydrophobicity of materials, providing improved water and stain resistance for coatings used in various industries, such as automotive, construction, and consumer goods.
Used in Polymer Synthesis:
(3-Methacryloyloxypropyl)trichlorosilane is used as a reactive compound in the synthesis of polymers, contributing to the development of new materials with enhanced properties, such as improved adhesion, durability, and hydrophobicity.
Used in Surface Modification:
(3-Methacryloyloxypropyl)trichlorosilane is used as a surface modifier to alter the properties of materials, such as enhancing their hydrophobicity, improving adhesion, or providing other functional properties for specific applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 7351-61-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,5 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7351-61:
(6*7)+(5*3)+(4*5)+(3*1)+(2*6)+(1*1)=93
93 % 10 = 3
So 7351-61-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H11Cl3O2Si/c1-6(2)7(11)12-4-3-5-13(8,9)10/h1,3-5H2,2H3

7351-61-3 Well-known Company Product Price

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  • Aldrich

  • (64205)  3-(Trichlorosilyl)propylmethacrylate  technical, ≥90% (GC)

  • 7351-61-3

  • 64205-5ML-F

  • 1,152.45CNY

  • Detail
  • Aldrich

  • (64205)  3-(Trichlorosilyl)propylmethacrylate  technical, ≥90% (GC)

  • 7351-61-3

  • 64205-25ML-F

  • 4,598.10CNY

  • Detail

7351-61-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-trichlorosilylpropyl 2-methylprop-2-enoate

1.2 Other means of identification

Product number -
Other names 2-Propenoic acid,2-methyl-,3-(trichlorosilyl)propyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
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:7351-61-3 SDS

7351-61-3Relevant articles and documents

Preparation of Organosilicon Compound Having (Meth)acryloyloxy Group

-

Paragraph 0063-0102; 0107-0110, (2021/05/14)

A (meth)acryloyloxy-containing organosilicon compound (3) is prepared by simultaneously feeding a hydrohalosilane compound (1) and a (meth)acrylate compound (2) in the presence of a polymerization inhibitor to a reaction system, and effecting hydrosilylation reaction in the presence of a platinum catalyst. The content of (meth)acrylate compound (2) is 0-100 mol % based on the content of organosilicon compound (3) in the reaction system. R is a C1-C10 monovalent hydrocarbon group, X is halogen, n is 1, 2 or 3, R2 is H or methyl, and R3 is a C1-C18 alkylene group.

Effect of catalysts on the reaction of allyl esters with hydrosilanes

Belyakova,Pomerantseva,Efimova,Chernyshev,Storozhenko

experimental part, p. 728 - 733 (2011/01/05)

The reaction of hydrosilylation of allyl esters XOCH 2CH=CH 2 (X = MeCO, CF 3CO, C 3F 7CO) and PhOCH 2CH=CH 2 with hydrosilanes HSiY 3 (Y = Cl, OEt) in the presence of the Speier catalyst, the Speier catalyst with additives, and of various nickel complexes was studied. The catalytic hydrosilylation reaction in the presence of the Speier catalyst is accompanied by the reduction. Additives to the Speier catalyst (vinyltriethoxysilane and some ethers) allow to suppress considerably the reduction reaction. In the presence of the studied nickel complexes mainly reduction and isomerization reactions occurred. The best nickel catalysts of hydrosilylation were the mixtures of NiCl 2 or Ni(acac) 2 with phosphine oxides. In contrast to allyl esters, the hydrosilylation of simple olefins proceeds easier, the content of the product of hydrosilylation in the reaction mixture reaches 94.3%. Pleiades Publishing, Ltd., 2010.

SYNTHESIS OF ORGANOSILICON DERIVATIVES OF ACRYLIC ACIDS

Efimov, Yu. T.,Tandura, T. A.,Kopylov, V. M.,Androsenko, S. I.,Shkol'nik, M. I.

, p. 2083 - 2091 (2007/10/02)

A study of the reactions of organohydrochlorosilanes with allyl acrylate showed that the addition proceeds at the β-position in all cases.The acrylate-containing chlorosilanes react with acetic anhydride to give quantitative yield of the acetoxy derivatives.Study of the hydrolysis of the chloro and acetoxy derivatives showed the feasibility of the direct synthesis of the corresponding silanols.The reactivity of these compounds was studied.

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