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14579-03-4

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14579-03-4 Usage

Description

CYCLOPENTYLTRICHLOROSILANE, also known as Trichloro(cyclopentyl)silane, is a polyhedral oligomeric silsesquioxane (POSS) derivative. It is synthesized through the hydrosilylation of cyclopentene and trichlorosilane, and is characterized by its potential to enhance the thermo-mechanical properties of various polymers.

Uses

Used in Polymer Industry:
CYCLOPENTYLTRICHLOROSILANE is used as a precursor for the preparation of POSS (polyhedral oligomeric silsesquioxane) through hydrolysis and condensation reactions. The application reason is to improve the thermo-mechanical properties of different polymers, making them more durable and resistant to high temperatures.

Check Digit Verification of cas no

The CAS Registry Mumber 14579-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,7 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14579-03:
(7*1)+(6*4)+(5*5)+(4*7)+(3*9)+(2*0)+(1*3)=114
114 % 10 = 4
So 14579-03-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H9Cl3Si/c6-9(7,8)5-3-1-2-4-5/h5H,1-4H2

14579-03-4 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (L16441)  Cyclopentyltrichlorosilane, 97%   

  • 14579-03-4

  • 25g

  • 887.0CNY

  • Detail
  • Alfa Aesar

  • (L16441)  Cyclopentyltrichlorosilane, 97%   

  • 14579-03-4

  • 100g

  • 3025.0CNY

  • Detail
  • Aldrich

  • (446181)  Trichlorocyclopentylsilane  95%

  • 14579-03-4

  • 446181-25ML

  • 1,139.58CNY

  • Detail

14579-03-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Trichlorocyclopentylsilane

1.2 Other means of identification

Product number -
Other names trichloro(cyclopentyl)silane

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:14579-03-4 SDS

14579-03-4Relevant articles and documents

Isolated SiH and GeH stretching frequencies and bond strength differences in cyclopropyl and cyclopentyl silanes and germanes

McKean, D. C.,Morrisson, A. R.,Dakkouri, M.

, p. 771 - 774 (1984)

Infrared gas phase spectra in the SiH and GeH stretching regions are reported for cyclopropyl-SiH3, -SiHD2, GeHD2, cyclopentyl-SiHD2 and -GeHD2.In each case two bands are seen which indicate the presence of stronger MHa and weaker MHs/sub

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

-

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.

Silane compound and processes for the preparation thereof

-

, (2008/06/13)

Novel silane compound, alkoxy cyclopentyl diethoxysilane, is prepared by reacting cyclopentyl trihalosilane with ROH and then with ethanol, or by reacting cyclopentyl triethoxysilane with ROH, wherein alkyl in the alkoxy or R in ROH stands for an organic group selected from tile group consisting of isopropyl, sec-butyl, tert-buryl and tert-amyl groups. The silane compounds are useful as a catalytic component for olefin polymerization and as a silane coupling agent.

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