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Triphenyl stannyl triphenyl silane is a chemical compound characterized by a tin atom connected to three phenyl groups and a silicon atom also connected to three phenyl groups. It is known for its role in organic synthesis, particularly as a cross-coupling reagent that facilitates the formation of carbon-carbon and carbon-heteroatom bonds. TRIPHENYL STANNYL TRIPHENYL SILANE is further utilized as a precursor in the synthesis of various organotin and organosilane compounds, as well as in the creation of functionalized silanes and other silicon-containing materials. Its potential applications extend to materials science, where it is being explored for its use in developing innovative polymers and nanocomposites.

6928-70-7

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6928-70-7 Usage

Uses

Used in Organic Synthesis:
Triphenyl stannyl triphenyl silane is used as a cross-coupling reagent for the formation of carbon-carbon and carbon-heteroatom bonds, which is crucial in the synthesis of complex organic molecules.
Used in the Preparation of Organotin and Organosilane Compounds:
It serves as a precursor in the synthesis of organotin and organosilane compounds, which are important in various chemical and industrial applications.
Used in the Synthesis of Functionalized Silanes:
Triphenyl stannyl triphenyl silane is utilized in the production of functionalized silanes, which are key components in the development of new materials with specific properties.
Used in Materials Science:
In the field of materials science, triphenyl stannyl triphenyl silane is used as a component in the development of new polymers and nanocomposites, contributing to advancements in material properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6928-70-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,2 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6928-70:
(6*6)+(5*9)+(4*2)+(3*8)+(2*7)+(1*0)=127
127 % 10 = 7
So 6928-70-7 is a valid CAS Registry Number.
InChI:InChI=1/C18H15Si.3C6H5.Sn/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;3*1-2-4-6-5-3-1;/h1-15H;3*1-5H;/rC18H15Si.C18H15Sn/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h2*1-15H

6928-70-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Triphenyl stannyl triphenyl silane

1.2 Other means of identification

Product number -
Other names Triphenyl-triphenylstannyl-silan

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:6928-70-7 SDS

6928-70-7Downstream Products

6928-70-7Relevant academic research and scientific papers

Cleavage of Sn-Sn Bonds in Hexaalkyl(aryl)stannanes under the Action of Yb(II) Derivatives

Syutkina,Rybakova,Novgorodova,Petrov

, p. 76 - 78 (2007/10/03)

Ytterbium(II) derivatives MeYbI, PhYbI, and YbI2 cleave the Sn-Sn bond in distannanes R′3-SnR′3 (R′ = n-Bu, Ph) to give heterobimetallic derivatives R′3SnYbI, which were identified by products of their hydrolysis, exchange with R″3EHlg (R″ = Ph, Me; E = Ge, Si, Sn) and cross coupling with MeI in the presence of NiCl2(Ph3P)2.

Electrochemical Formation of Dimeric Organostannyl Compounds

Ishiwata, Toyoaki,Nonaka, Tsutomu,Umezawa, Masanobu

, p. 1631 - 1634 (2007/10/02)

Organosilyl stannanes were formed by electroreduction of the corresponding organostannyl chlorides or distannanes with silyl chlorides.The Sn-C bond formation was also confirmed in the reduction of a mixture of stannyl and alkyl chlorides.

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