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CAS

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18001-13-3

(4-ethenylphenyl) trimethoxy-Silane, also known as vinyltrimethoxysilane, is a chemical compound with the formula C11H16O3Si. It is a versatile coupling agent and adhesion promoter derived from the reaction of vinyl chloride and methanol, playing a crucial role in enhancing the bonding of organic polymers to inorganic materials.

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  • 18001-13-3 Structure

  • Basic information

    1. Product Name: (4-ethenylphenyl) trimethoxy-Silane
    2. Synonyms: (4-ethenylphenyl) trimethoxy-Silane;Silane,(4-ethenylphenyl)trimethoxy-;Trimethoxy(4-vinylphenyl)silane;p-styryltrimethoxysilane
    3. CAS NO:18001-13-3
    4. Molecular Formula: C11H16O3Si
    5. Molecular Weight: 224.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 18001-13-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 77°C/0.2mmHg(lit.)
    3. Flash Point: 136°C (277°F)
    4. Appearance: /
    5. Density: 1.057 g/cm3(Temp: 25 °C)
    6. Refractive Index: 1.5050 to 1.5090
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (4-ethenylphenyl) trimethoxy-Silane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-ethenylphenyl) trimethoxy-Silane(18001-13-3)
    11. EPA Substance Registry System: (4-ethenylphenyl) trimethoxy-Silane(18001-13-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 18001-13-3(Hazardous Substances Data)

18001-13-3 Usage

Uses

Used in Plastic and Rubber Industries:
(4-ethenylphenyl) trimethoxy-Silane is used as a coupling agent and adhesion promoter for improving the bonding of organic polymers to inorganic materials, such as in the production of composite materials.
Used in Manufacturing of Adhesives and Sealants:
(4-ethenylphenyl) trimethoxy-Silane is used as a key component in the formulation of adhesives and sealants, contributing to their enhanced performance and durability.
Used in Surface Modification:
(4-ethenylphenyl) trimethoxy-Silane is used as a surface modifier for glass and metal substrates, providing improved adhesion and compatibility with various materials.
Used in Functionalization of Nanoparticles:
(4-ethenylphenyl) trimethoxy-Silane is used for the functionalization of nanoparticles, enabling their integration into various applications, such as drug delivery systems and coatings.
Handling and Storage:
Due to its reactivity with moisture, (4-ethenylphenyl) trimethoxy-Silane must be handled and stored with care in a dry and controlled environment to ensure its stability and performance.

Check Digit Verification of cas no

The CAS Registry Mumber 18001-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,0 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18001-13:
(7*1)+(6*8)+(5*0)+(4*0)+(3*1)+(2*1)+(1*3)=63
63 % 10 = 3
So 18001-13-3 is a valid CAS Registry Number.

18001-13-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-ethenylphenyl)-trimethoxysilane

1.2 Other means of identification

Product number -
Other names KBM1403

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:18001-13-3 SDS

18001-13-3Relevant articles and documents

Directed palladium(II)-catalyzed intermolecular anti-markovnikov hydroarylation of unactivated alkenes with (hetero)arylsilanes

Lu, Ming-Zhu,Loh, Teck-Peng,Luo, Haiqing,Hu, Zhengsong,Shao, Changdong,Kan, Yuhe

supporting information, p. 9022 - 9028 (2020/12/02)

We describe herein a regioselective palladium(II)catalyzed intermolecular hydroarylation of unactivated aliphatic alkenes with electronically and sterically diverse (hetero)arylsilanes under redox-neutral conditions. A removable bidentate 8-amino-quinoline auxiliary was readily employed to dictate the regioselectivity, prevent β-hydride elimination, and facilitate protodepalladation. This silicon-based protocol features a broad substrate scope with excellent functional group compatibility and enables an expeditious route to a variety of γ-aryl butyric acid derivatives in good yields with exclusive anti-Markovnikov selectivity.

Method for preparing styryl-functionalized silanes

-

, (2008/06/13)

The invention relates to a method for preparing silanes comprising styryl groups, said silanes being represented by the general formula (I): (St) bSiR′aR4?a?b with improved yields through a reaction with magnesium in a sol

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