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Silane, difluoro-1-naphthalenylphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63322-24-7

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63322-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63322-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,2 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63322-24:
(7*6)+(6*3)+(5*3)+(4*2)+(3*2)+(2*2)+(1*4)=97
97 % 10 = 7
So 63322-24-7 is a valid CAS Registry Number.

63322-24-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name difluoro-(1-naphthalen-1-ylcyclohexa-2,4-dien-1-yl)silicon

1.2 Other means of identification

Product number -
Other names Silane,difluoro-1-naphthalenylphenyl

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:63322-24-7 SDS

63322-24-7Downstream Products

63322-24-7Relevant academic research and scientific papers

Electrochemical properties of arylsilanes

Biedermann, Judith,Wilkening, H. Martin R.,Uhlig, Frank,Hanzu, Ilie

, p. 13 - 18 (2019/03/27)

In the past, the electrochemical properties of organosilicon compounds were investigated for both fundamental reasons and synthesis purposes. Little is, however, known about the electrochemical behaviour of hydrogen-bearing arylsilanes. Here, we throw light on the electrochemical properties of 11 arylsilanes compounds, 2 of them synthesized for the first time. The oxidation potentials are found to depend on both the nature and number of the aryl groups. Based on these findings it was possible to establish some variation trends that match the expected structure–property correlations. Furthermore, we present first insights into the electrochemical reaction kinetics behind and identify several soluble electrochemical oxidation products.

USE OF SbF5 INTERCALATED IN GRAPHITE AS FLUORINATING REAGENT IN ORGANO-SILICON AND -GERMANIUM CHEMISTRY

Corriu, R.J.P.,Fernandez, J.M.,Guerin, C.

, p. 347 - 352 (2007/10/02)

The use of SbF5 intercalated in graphite as fluorinating reagent of organo-silicon and -germanium derivatives is described.While Si-O and Si-Cl bonds are readily cleaved, Si-H and Si-S bonds are only reactive in bifunctional silanes.Ge-X bonds (X=Br, Cl, OR, H) are unreactive.Allyl-silicon and allyl-germanium bonds are broken under mild conditions and in high yields, leading to the corresponding fluorosilane or fluorogermane.With bifunctional silanes, it is always possible to obtain the difluorinated derivatives.

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