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2-(BICYCLOHEPTYL)TRICHLOROSILANE is a chemical compound characterized by the attachment of a trichlorosilane group to a bicycloheptyl group. It is known for its high reactivity, which allows it to engage in a variety of reactions with organic compounds. Due to its corrosive nature, it necessitates careful handling and the use of personal protective equipment to prevent skin and eye irritation.

18245-29-9

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18245-29-9 Usage

Uses

Used in Organic Synthesis:
2-(BICYCLOHEPTYL)TRICHLOROSILANE is utilized as a reagent in organic synthesis for its ability to participate in a broad spectrum of chemical reactions, making it a valuable component in the creation of diverse organic compounds.
Used as a Precursor in Silicon-Containing Materials:
In the field of material science, 2-(BICYCLOHEPTYL)TRICHLOROSILANE serves as a precursor for the development of various silicon-containing materials, leveraging its reactivity to form new compounds with potential applications in different industries.
Used in Chemical Research:
2-(BICYCLOHEPTYL)TRICHLOROSILANE is also employed in chemical research as a tool to explore and understand the reactivity and bonding capabilities of trichlorosilane groups with different organic substrates, contributing to the advancement of chemical knowledge and technology.
Used in the Production of Specialty Coatings:
In the coatings industry, 2-(BICYCLOHEPTYL)TRICHLOROSILANE is used as a component in the formulation of specialty coatings that may benefit from the unique properties conferred by silicon-containing compounds, such as enhanced durability and resistance to environmental factors.
Used in the Semiconductor Industry:
The semiconductor industry may utilize 2-(BICYCLOHEPTYL)TRICHLOROSILANE in the manufacturing process of electronic components, taking advantage of its reactivity and silicon content to create materials with specific electrical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 18245-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,4 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18245-29:
(7*1)+(6*8)+(5*2)+(4*4)+(3*5)+(2*2)+(1*9)=109
109 % 10 = 9
So 18245-29-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H11Cl3Si/c8-11(9,10)7-4-5-1-2-6(7)3-5/h5-7H,1-4H2

18245-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bicyclo[2.2.1]heptanyl(trichloro)silane

1.2 Other means of identification

Product number -
Other names 2-Trichlorsilyl-bicyclo-<2.2.1>-heptan

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:18245-29-9 SDS

18245-29-9Relevant academic research and scientific papers

[3-(2-NORBORNYL)-2-NORBORNYL]SILANE COMPOUND AND MAKING METHOD

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Paragraph 0069; 0070; 0071, (2014/05/08)

A [3-(2-norbornyl)-2-norbornyl]silane compound having formula (1) is novel, wherein R1 is a monovalent hydrocarbon radical, X is halogen or an organoxy OR2, R2 is a monovalent hydrocarbon radical, n is 1 or 2 when X is halogen, and n is 0, 1 or 2 when X is organoxy. It is a useful reactant for forming surface coatings on electronic parts.

Trichlorosilyl groups containing organochlorosilanes and their preparation methods by the double-silylation of olefins with trichlorosilane

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Page 5, (2008/06/13)

The present invention provides organosilicon compounds containing two trichlorosilyl groups and their preparation methods. Organosilicon compounds of formula II are prepared by reacting linear chain or cyclic olefins of formula I with trichlorosilane in the presence of quaternary organophosphonium salt as a catalyst.R1—HC=CH—R2??(I) 1In formulas I and II, R1 and R2 may be identical or different and represent a hydrogen atom, a linear or a cyclic C1-C8 alkyl, a linear or a cyclic C1-C8 alkenyl, benzyl, phenyl, a C1-C8 alkyl substituted phenyl group, two functional groups between R1 and R2 may be covalently bonded to form a C4-C8 ring with or without a carbon-carbon double bond.

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