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Triphenyl(2,3,4-triphenylcyclopentadienylidene)arsorane is a complex organic compound with the chemical formula C45H30As. It is a derivative of arsabenzene, which is an organoarsenic compound that contains a cyclopentadienyl ligand. The molecule consists of a central arsenic atom bonded to three phenyl rings and a cyclopentadienyl ring, which is further substituted with three additional phenyl groups. Triphenyl(2,3,4-triphenylcyclopentadienylidene)arsorane is of interest in organometallic chemistry due to its unique structure and potential applications in materials science and catalysis. However, it is important to note that organoarsenic compounds can be toxic, and their handling should be done with proper safety precautions.

33974-66-2

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33974-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33974-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,9,7 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 33974-66:
(7*3)+(6*3)+(5*9)+(4*7)+(3*4)+(2*6)+(1*6)=142
142 % 10 = 2
So 33974-66-2 is a valid CAS Registry Number.

33974-66-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Triphenyl(2,3,4-triphenylcyclopentadienylidene)arsorane

1.2 Other means of identification

Product number -
Other names Triphenylarsonium-2,3,4-triphenylcyclopentadienylid

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:33974-66-2 SDS

33974-66-2Relevant academic research and scientific papers

A Gentle Method for the Preparation of a Variety of Ylides (As, Sb, Bi, S, Te, Thiouronium) from Diazo Compounds

Glidewell, Christopher,Lloyd, Douglas,Metcalfe, Shirley

, p. 319 - 321 (2007/10/02)

Bis(hexafluoroacetylacetonato)copper(II) is a very effective catalyst for the preparation of ylides from diazo compounds under mild conditions even down to room temperature.It appears that the lower the temperature at which the reaction can be conducted the purer the product which results.Its use in preparing arsonium, stibonium, bismuthonium, sulphonium, telluronium, and thiouronium ylides is described.

TRITOLYLARSONIUM AND TRIS(METHOXYPHENYL)ARSONIUM YLIDES THE EFFECTS OF ortho-SUBSTITUENTS IN TRIARYLARSONIUM GROUPS ON THE PROPERTIES OF YLIDES

Harris, Gordon S.,Lloyd, Douglas,MacDonald, William A.,Gosney, Ian

, p. 297 - 304 (2007/10/02)

A number of tritolylarsonium and tris(methoxyphenyl)arsonium cyclopentadienylides and other ylides have been prepared and their properties (basicity, NMR spectra, reactions with aldehydes and nitrosobenzene, acetylation, and methanolysis) have been investigated.Substituents in the m- or p-positions of triarylarsonium groups have little effect on properties, but o-substituents result in markedly lower reactivity and lower basicity, and these ylides were also more difficult to prepare.NMR spectra gave indication of crowding in some of these o-substituted ylides.The effects of the o-substituents are discussed. p-Methyl- and p-methoxy-substituents increased the proportion of anil to ketoxime formed in reactions with nitrosobenzene, but the o-methoxy analogue gave only ketoxime.

THE EFFECTS OF DIFFERENT COPPER (AND SOME OTHER) CATALYSTS ON THE CONVERSION OF TRIPHENYL- AND TETRAPHENYL-DIAZOCYCLOPENTADIENES AND OF SOME PHENYLIODONIUM αα'-DICARBONYLYLIDES INTO ARSONIUM AND OTHER YLIDES

Hood, J. Nicholas C.,Lloyd, Douglas,MacDonald, William A.,Shepherd, T. Maurice

, p. 3355 - 3358 (2007/10/02)

Diazo-compounds or iodonium ylides may be converted into arsonium and other ylides when heated in solution with triphenylarsine or other suitable carbene (or carbenoid) acceptor, and with a suitable Cu derivative present.The effects of using different copper complexes and salts are described and discussed.Other metal derivatives were for the most part ineffetive as catalysts.

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