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Diphenylstibane is an organostibine compound with the chemical formula (C6H5)2Sb. It is a derivative of stibine, where two phenyl groups (C6H5) are attached to the antimony atom. Diphenylstibane is a colorless, crystalline solid that is sensitive to air and moisture, and it has a pungent odor. diphenylstibane is of interest in organometallic chemistry and is used in the synthesis of various organostibine compounds. It is typically synthesized by reacting antimony trichloride with lithium phenyl, and its properties, such as reactivity and stability, are influenced by the presence of the phenyl groups. Diphenylstibane is also known for its potential applications in materials science and as a precursor in the preparation of other organostibine compounds.

5865-81-6

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5865-81-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5865-81-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,6 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5865-81:
(6*5)+(5*8)+(4*6)+(3*5)+(2*8)+(1*1)=126
126 % 10 = 6
So 5865-81-6 is a valid CAS Registry Number.

5865-81-6SDS

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 diphenylstibane

1.2 Other means of identification

Product number -
Other names Diphenylstiban

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:5865-81-6 SDS

5865-81-6Relevant articles and documents

Oxidative addition across sb-h and sb-sb bonds by an osmium carbonyl cluster: Trapping the intermediate

Li, Ying-Zhou,Ganguly, Rakesh,Leong, Weng Kee

, p. 823 - 828 (2014/03/21)

The cluster Os3(CO)11(NCCH3) oxidatively adds across the Sb-H bond in SbPh2H to afford the clusters Os 3(CO)11(H)(μ-SbPh2) and Os 3(CO)11(μ-H)(μ-SbPh2)Os 3(CO)11. Similarly, its reaction with Sb 2Ph4 afforded Os3(CO)11(μ- SbPh2)2Os3(CO)11 as the major product. In both cases, the intermediate from the oxidative addition reaction was trapped as a W(CO)5 adduct.

Electrochemical studies on organometallic compounds XXXVI. New aspects of the electroreduction of (Ph2Sb)2O, (Ph2Sb)2, Ph2Sb(nBu), and Ph3Sb

Mourad, Y.,Mugnier, Y.,Breunig, H.J.,Ates, M.

, p. 85 - 90 (2007/10/02)

Electroreduction of (Ph2Sb)2O (1) in THF gives Ph2Sb-, which can also be obtained by uptake of two electrons on (Ph2Sb)2 (2).Ph2Sb- reacts with the supporting salt (nBu4NPF6) to yield tributylamine and Ph2Sb(nBu) (3).The electroreduction of 3 and Ph3Sb (4) gives also the anion Ph2Sb-.There is a considerable influence of the electrode surface on the redox properties of 1-4.Mechanistic aspects are discussed.

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.

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