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(M-TERPHENYL-5'-YL)TRIMETHYLSILANE, with the molecular formula C21H22Si, is a silane compound characterized by a trimethylsilyl group attached to a m-terphenyl-5'-yl moiety. It is a versatile chemical entity with applications in various fields of chemistry and materials science.

128388-53-4

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128388-53-4 Usage

Uses

Used in Organic Synthesis:
(M-TERPHENYL-5'-YL)TRIMETHYLSILANE is used as a reagent in organic synthesis for its ability to facilitate specific chemical reactions, contributing to the formation of desired products with enhanced efficiency and selectivity.
Used in Transition Metal Catalysis:
In the field of catalysis, (M-TERPHENYL-5'-YL)TRIMETHYLSILANE serves as a ligand, enhancing the catalytic activity of transition metals. Its unique structure allows it to stabilize and modulate the reactivity of metal centers, leading to improved catalytic processes.
Used in the Synthesis of Functional Materials:
(M-TERPHENYL-5'-YL)TRIMETHYLSILANE is utilized as a building block in the synthesis of various functional materials. Its incorporation into these materials can impart specific properties, such as improved stability, reactivity, or selectivity, depending on the application.
Used in Pharmaceutical Industry:
(M-TERPHENYL-5'-YL)TRIMETHYLSILANE is used as a key intermediate in the synthesis of pharmaceuticals. Its unique structural features can be leveraged to develop new drugs with enhanced therapeutic properties or to improve the synthesis processes of existing medications.

Check Digit Verification of cas no

The CAS Registry Mumber 128388-53-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,3,8 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 128388-53:
(8*1)+(7*2)+(6*8)+(5*3)+(4*8)+(3*8)+(2*5)+(1*3)=154
154 % 10 = 4
So 128388-53-4 is a valid CAS Registry Number.

128388-53-4SDS

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 Trimethyl(m-terphenyl-5'-yl)silane

1.2 Other means of identification

Product number -
Other names (3,5-diphenylphenyl)-trimethylsilane

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:128388-53-4 SDS

128388-53-4Relevant academic research and scientific papers

Optically active dendrimers with a binaphthyl core and phenylene dendrons: Light harvesting and enantioselective fluorescent sensing

Gong,Hu,Pu

, p. 2358 - 2367 (2007/10/03)

Optically active dendrimers containing a 1,1′-binaphthyl core and cross-conjugated phenylene dendrons were synthesized and characterized. The chiral optical properties of these phenylene-based dendrimers are different from the previously reported phenyleneethynylene-based dendrimers probably because of the increased steric interaction between the adjacent phenylene units. UV and fluorescence spectroscopic studies demonstrate that the energy harvested by the periphery of the dendrimers can be efficiently transferred to the more conjugated core, generating much enhanced fluorescence signal at higher generation. The fluorescence of these dendrimers can be quenched both efficiently and enantioselectively by chiral amino alcohols. The energy migration and light-harvesting effects of the dendrimers make the higher generation dendrimer more sensitive to fluorescent quenchers than the lower ones. Thus, the dendritic structure provides a signal amplification mechanism. These materials are potentially useful in the enantioselective recognition of chiral organic molecules.

Synthesis and characterization of a series of monodisperse, 1,3,5-phenylene-based hydrocarbon dendrimers including C276H186 and their fluorinated analogues

Miller, Timothy M.,Neenan, Thomas X.,Zayas, Roberto,Bair, Harvey E.

, p. 1018 - 1025 (2007/10/02)

The convergent synthesis of a series of monodisperse aromatic dendrimers having molecular diameters of 15-31 ? is described. These materials consist of 4, 10, 22, or 46 benzene rings linked symmetrically by σ-bonds. Increasingly large dendrimer arms are p

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