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Carbazolepropyltriethoxysilane is a versatile chemical compound that features a carbazole group, a propyl group, and three triethoxysilane groups. It is recognized for its ability to function as a coupling agent and surface modifier, enhancing the adhesion and compatibility between organic and inorganic materials. carbazolepropyltriethoxysilane is also valued for its potential to improve the mechanical and thermal properties of materials, as well as for its high thermal stability and electrical properties, making it suitable for electronic and optoelectronic applications. Furthermore, carbazolepropyltriethoxysilane holds promise for the preparation of functionalized surfaces in biotechnology and analytical chemistry.

221105-38-0

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221105-38-0 Usage

Uses

Used in Polymer and Composite Production:
Carbazolepropyltriethoxysilane is used as a coupling agent and surface modifier to improve the adhesion and compatibility between organic and inorganic materials in the production of polymers and composites. This enhances the mechanical and thermal properties of the resulting products.
Used in Coating Industry:
In the coating industry, carbazolepropyltriethoxysilane is utilized as a coupling agent to enhance the adhesion of coatings to various substrates, thereby improving the durability and performance of the coatings.
Used in Electronic and Optoelectronic Applications:
Carbazolepropyltriethoxysilane is employed in the preparation of materials for electronic and optoelectronic applications due to its high thermal stability and electrical properties, which are crucial for the performance of these devices.
Used in Biotechnology and Analytical Chemistry:
In the fields of biotechnology and analytical chemistry, carbazolepropyltriethoxysilane is used in the preparation of functionalized surfaces, which can be tailored for specific applications, such as biosensors or other analytical devices.
Overall, carbazolepropyltriethoxysilane is a multifaceted chemical with a broad spectrum of applications across various industries, from material science to electronics, and holds potential for further development and utilization in research and commercial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 221105-38-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,1,0 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 221105-38:
(8*2)+(7*2)+(6*1)+(5*1)+(4*0)+(3*5)+(2*3)+(1*8)=70
70 % 10 = 0
So 221105-38-0 is a valid CAS Registry Number.

221105-38-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name carbazolepropyltriethoxysilane

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:221105-38-0 SDS

221105-38-0Downstream Products

221105-38-0Relevant academic research and scientific papers

(Dicyclopentadiene) platinum(II) dichloride: An efficient catalyst for the hydrosilylation reaction between alkenes and triethoxysilane

Wu, Huarui,Zheng, Chaoyue,Chen, Naiwu,Zhu, Jie,Gao, Deqing

, p. 1576 - 1578 (2017)

(Dicyclopentadiene) platinum(II) dichloride was found to be an efficient hydrosilylation catalyst (homogeneous) upon a wide variety of functionalized alkenes and alkenes terminated with chemical moieties (diphenyl amino-, N-carbazol- and N-isoindoline-1,3-dione-). It is noteworthy that the hydrosilylation of aminated alkenes with triethoxysilane exhibited the yield of over 70% and the selectivity (γ-isomer/β-isomer) of more than 3/1. Due to steric hindrance lowering Markovnikov probability, the alkenes with big terminal moieties (diphenyl amino-, N-carbazol- and N-isoindoline-1,3-dione-) presented the high ratio of anti-Markovnikov isomers. The strategy of the hydrosilylation of the protected diamino chelating alkene was developed.

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