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11-Azidoundecyltriethoxysilane, 95% is a chemical compound that is primarily used as a coupling agent in various applications. It is characterized by its ability to specifically react with alkyne functions to form the corresponding 1,2,3-triazole through a copper-free 1,3-dipolar cycloaddition process.

663171-33-3

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663171-33-3 Usage

Uses

Used in Chemical Synthesis:
11-Azidoundecyltriethoxysilane, 95% is used as a coupling agent for chemical synthesis, particularly in the formation of 1,2,3-triazoles via a copper-free 1,3-dipolar cycloaddition. This application is significant because it allows for the creation of new chemical compounds with potential applications in various industries.
Used in Material Science:
In the field of material science, 11-Azidoundecyltriethoxysilane, 95% is used as a coupling agent to enhance the properties of materials. Its ability to form 1,2,3-triazoles with alkyne functions can improve the stability, strength, and durability of certain materials, making them more suitable for specific applications.
Used in Pharmaceutical Industry:
11-Azidoundecyltriethoxysilane, 95% is also used as a coupling agent in the pharmaceutical industry. Its role in the formation of 1,2,3-triazoles can contribute to the development of new drugs with improved efficacy and reduced side effects. This application is particularly important in the ongoing search for novel therapeutic agents to treat various diseases and conditions.
Used in Nanotechnology:
In nanotechnology, 11-Azidoundecyltriethoxysilane, 95% is utilized as a coupling agent to facilitate the creation of nanomaterials with specific properties. The formation of 1,2,3-triazoles through a copper-free 1,3-dipolar cycloaddition can lead to the development of advanced nanostructures with potential applications in electronics, energy storage, and other high-tech industries.
Overall, 11-Azidoundecyltriethoxysilane, 95% is a versatile coupling agent with a wide range of applications across different industries, including chemical synthesis, material science, pharmaceuticals, and nanotechnology. Its ability to form 1,2,3-triazoles with alkyne functions makes it a valuable tool in the development of new compounds, materials, and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 663171-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,3,1,7 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 663171-33:
(8*6)+(7*6)+(6*3)+(5*1)+(4*7)+(3*1)+(2*3)+(1*3)=153
153 % 10 = 3
So 663171-33-3 is a valid CAS Registry Number.

663171-33-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H33524)  11-Azidoundecyltriethoxysilane, 95%   

  • 663171-33-3

  • 250mg

  • 1245.0CNY

  • Detail
  • Alfa Aesar

  • (H33524)  11-Azidoundecyltriethoxysilane, 95%   

  • 663171-33-3

  • 1g

  • 3450.0CNY

  • Detail

663171-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-azido-n-undecyltriethoxysilane

1.2 Other means of identification

Product number -
Other names -

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:663171-33-3 SDS

663171-33-3Relevant academic research and scientific papers

Organosilica-metallic sandwich materials as precursors for palladium and platinum nanoparticle synthesis

Besnard, Romain,Cambedouzou, Julien,Arrachart, Guilhem,Le Goff, Xavier F.,Pellet-Rostaing, Stéphane

, p. 77619 - 77628 (2015/09/28)

A promising strategy to design highly active catalysts is to use multicomponent catalysts including active metals (such as platinoids) and organosilica as a substrate. In this article, we develop stable OrganoSilica Sandwiches (OSS) consisting of sandwiched metallic layers between organosilica layers. The formation of such a sandwich-like organosilica@platinoid@organosilica material was obtained from bis-silica-alkylammonium carbamate dimers, acting as a template for the immobilization of platinoid salt complexes or metallic nanoparticles in the interlayer space after a reduction treatment. The layered templates and the sandwich structures were investigated by small angle X-ray scattering, coupled thermogravimetric analysis and mass spectrometry, and Raman spectroscopy. It was demonstrated that the meso-structure of the initial template material is not affected by the chemical steps involved in the synthesis of the material and does not depend on the incorporated metal.

Preparation of bifunctional mesoporous silica nanoparticles by orthogonal click reactions and their application in cooperative catalysis

Dickschat, Arne T.,Behrends, Frederik,Bühner, Martin,Ren, Jinjun,Wei?, Mark,Eckert, Hellmut,Studer, Armido

supporting information, p. 16689 - 16697 (2013/03/14)

The synthesis of bifunctional mesoporous silica nanoparticles is described. Two chemically orthogonal functionalities are incorporated into mesoporous silica by co-condensation of tetraethoxysilane with two orthogonally functionalized triethoxyalkylsilanes. Post-functionalization is achieved by orthogonal surface chemistry. A thiol-ene reaction, Cu-catalyzed 1,3-dipolar alkyne/azide cycloaddition, and a radical nitroxide exchange reaction are used as orthogonal processes to install two functionalities at the surface that differ in reactivity. Preparation of mesoporous silica nanoparticles bearing acidic and basic sites by this approach is discussed. Particles are analyzed by solid state NMR spectroscopy, elemental analysis, infrared-spectroscopy, and scanning electron microscopy. As a first application, these particles are successfully used as cooperative catalysts in the Henry reaction. Cooperative clicking: Bifunctional mesoporous silica particles were synthesized by orthogonal surface chemistry. A thiol-ene reaction, a copper-catalyzed 1,3-dipolar cycloaddition and a radical nitroxide exchange reaction were used as orthogonal processes for the introduction of the acid and base functionalities (see scheme). Catalytic activities of these bifunctionalized inorganic/organic hybrid materials were studied on the Henry reaction. Copyright

A simple access to ω-aminoalkyltrialkoxysilanes: Tunable linkers for self-organised organosilicas

Pichon, Beno?t P.,Wong Chi Man, Michel,Bied, Catherine,Moreau, Jo?l J.E.

, p. 1126 - 1130 (2007/10/03)

A simple route to ω-aminoalkyltriethoxysilanes with variable alkylene chain lengths, (EtO)3Si(CH2)nNH2 (n = 5, 11) is described. These silyl linkers have been used to prepare urea-based compounds with H-bonding and hydrophobic interactions which enable the self-assembly of the molecules. These molecular precursors are suitable for the obtention of nano-structured hybrid silicas.

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