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18858-75-8

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18858-75-8 Usage

General Description

(4-methylphenyl)(triphenyl)silane is a chemical compound with the molecular formula C25H24Si. It is a silane derivative, consisting of a silicon atom bonded to three phenyl groups and one 4-methylphenyl group. This chemical is commonly used as a building block for the synthesis of various organosilicon compounds. It has applications in materials science, as a precursor for the production of siloxane polymers and as a starting material for the synthesis of functionalized silanes. Its unique structure and properties make it a valuable tool in the development of advanced materials and other technological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 18858-75-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,5 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18858-75:
(7*1)+(6*8)+(5*8)+(4*5)+(3*8)+(2*7)+(1*5)=158
158 % 10 = 8
So 18858-75-8 is a valid CAS Registry Number.

18858-75-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methylphenyl)-triphenylsilane

1.2 Other means of identification

Product number -
Other names 1-Methyl-3-triphenylsilyl-benzol

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:18858-75-8 SDS

18858-75-8Relevant articles and documents

Regiocontrolled cobalt-catalyzed Diels-Alder reactions of silicon-functionalized, terminal, and internal alkynes

Hilt, Gerhard,Janikowski, Judith

supporting information; experimental part, p. 773 - 776 (2009/08/19)

(Chemical Equation Presented) The efficient control of the regiochemistry of the Diels-Alder adducts which are formed in excellent yields from 1,3-dienes and alkynylsilanes can be realized utilizing cobalt complexes with a pyridine-imine ligand or a dppe ligand, respectively. The application of 2-trimethylsilyloxy-1,3-butadiene leads to a very interesting cyclohexenone derivative suitable for further transformations.

Catalytic process for producing silahydrocarbons

-

, (2008/06/13)

Silahydrocarbons such as tetraorganosilanes prepared from halo-substituted silanes and an organomagnesium compound in the presence of a catalytically effective amount of a cyanide.

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