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69561-88-2

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69561-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69561-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,5,6 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69561-88:
(7*6)+(6*9)+(5*5)+(4*6)+(3*1)+(2*8)+(1*8)=172
172 % 10 = 2
So 69561-88-2 is a valid CAS Registry Number.
InChI:InChI=1/2C6H5.C3H9Si.Sb/c2*1-2-4-6-5-3-1;1-4(2)3;/h2*1-5H;1-3H3;/rC12H10Sb.C3H9Si/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12;1-4(2)3/h1-10H;1-3H3

69561-88-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name diphenylantimony,trimethylsilicon

1.2 Other means of identification

Product number -
Other names -

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:69561-88-2 SDS

69561-88-2Relevant articles and documents

NEUE DARSTELLUNG, SCHWEFELINSERTION UND HYDROLYSE DER PHENYL(TRIMETHYLSILYL)STIBANE

Ates, M.,Breunig, H. J.,Guelec, S.

, p. 129 - 134 (2007/10/02)

Reaction of Mg and Me3SiCl with Ph2SbCl or PhSbCl2 gives Ph2SbSiMe3 (1) or PhSb(SiMe3)2 (2).Sulfur inserts into 1 to give Ph2SbSSiMe3 (3).Products of action of S8 on 2 are 3, PhSb(SSiMe3)2 (4), (Me3Si)2S, and Sb2S3.Hydrolysis or methanolysis of 1, or 2 give Ph2SbH (5), or PhSbH2 (6), respectively.Key words: Diphenyl(trimethylsilyl)stibane; phenylbis(trimethylsilyl)stibane; diphenyl(trimethylsilyl-thio)stibane; diphenylstibane; phenylstibane.

Diphenylarsinoderivatives of Maleic Acid Anhydride and Related Compounds. Crystal and Molecular Structure of 2,3-Bis(diphenylstibino)maleic Acid Anhydride

Fenske, Dieter,Teichert, Heinz,Prokscha, Heinz,Renz, Werner,Becher, Hermann J.

, p. 177 - 192 (2007/10/02)

The unusual properties of bis(diphenylphosphino)maleic anhydride and similar ditertiary phosphines has prompted the synthesis of analogous arsines and stibines.Bis(diphenylarsino)maleic anhydride, -maleic thioanhydride and -N-methyl maleic imide, bis(diphenylstibino)maleic anhydride (5) and -maleic thioanhydride are obtained as crystalline yellow or red compounds by the reaction of the corresponding 2,3-dichloromaleic acid derivatives with diphenyl(trimethylsilyl)arsine and -stibine resp.The uv/vis spectra and characteristic i.r. bands of selected compounds are given and compared with those of the corresponding phosphines.The strong shift of νC=C to lower wavenumbers observed in all compounds has caused the determination of crystal and molecular structure of 5 by x-ray diffraction.Bond distances and angles are given.The complex formation of the new diarsine ligands has been examined by the preparation of Ni-, Cr- and Mo-carbonyl derivatives.As the first organylsulfane substituted maleic acid derivatives bis(phenylthio)maleic thioanhydride, -N-methyl-maleic imide and -maleic acid dimethylester are synthesized and described. - Keywords: Bis(diphenylarsino)maleic acid, derivatives; Bis(diphenylstibino)maleic anhydride, synthesis, crystal structure; Bis(phenylthio)maleic acid, derivatives; Maleic acid derivatives, synthesis, molecular structure

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