18858-72-5 Usage
Description
(3-methylphenyl)(triphenyl)silane, also known as triphenyl(3-methylphenyl)silane, is a chemical compound with the molecular formula C28H24Si. It consists of a silicon atom bonded to three phenyl groups and one 3-methylphenyl group. This organosilicon compound is characterized by its unique structure, which allows it to serve as a source of both the phenyl and 3-methylphenyl groups in various chemical reactions.
Uses
Used in Organic Synthesis:
(3-methylphenyl)(triphenyl)silane is used as a reagent in organic synthesis for its ability to provide both phenyl and 3-methylphenyl groups. This makes it a versatile building block for the creation of a wide range of organic compounds.
Used in the Preparation of Organosilicon Compounds:
As a building block, (3-methylphenyl)(triphenyl)silane is utilized in the synthesis of other organosilicon compounds, which have diverse applications in various industries.
Used in the Development of Optical and Electronic Materials:
(3-methylphenyl)(triphenyl)silane is used as a component in the development of materials with specific optical and electronic properties. Its structure contributes to the performance of these materials, making it suitable for applications such as light-emitting diodes and organic semiconductors.
Used in Pharmaceutical and Medicinal Applications:
(3-methylphenyl)(triphenyl)silane has been investigated for its potential use in pharmaceutical and medicinal applications, capitalizing on its unique chemical properties to contribute to the development of new drugs and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 18858-72-5 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 18858-72:
(7*1)+(6*8)+(5*8)+(4*5)+(3*8)+(2*7)+(1*2)=155
155 % 10 = 5
So 18858-72-5 is a valid CAS Registry Number.
18858-72-5Relevant 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.
