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Triphenylarsane sulfide, also known as arsenic triphenyl sulfide, is an organoarsenic compound characterized by the chemical formula C18H15AsS. It presents as a yellow solid with a distinct garlic-like odor. triphenylarsane sulfide is recognized for its role as a reagent in organic chemistry, particularly in the synthesis of various organoarsenic compounds. Its versatility extends to potential applications as a pesticide and in certain industrial processes, although its use is tempered by its toxic nature, which necessitates careful handling to avoid adverse health effects.

3937-40-4

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3937-40-4 Usage

Uses

Used in Organic Chemistry:
Triphenylarsane sulfide is utilized as a reagent for the synthesis of a range of organoarsenic compounds, contributing to the advancement of chemical research and the development of new materials.
Used in Pesticide Formulations:
Recognized for its pesticidal potential, triphenylarsane sulfide is employed as an active ingredient in some pesticide formulations, aiming to control and manage pests in agricultural settings.
Used in Industrial Processes:
triphenylarsane sulfide also finds application in specific industrial processes, where its unique properties are leveraged to achieve desired outcomes in manufacturing and production.
It is crucial to note that due to the toxic nature of triphenylarsane sulfide, it should be handled with appropriate safety measures to prevent skin and eye irritation as well as more severe health consequences.

Check Digit Verification of cas no

The CAS Registry Mumber 3937-40-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,3 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3937-40:
(6*3)+(5*9)+(4*3)+(3*7)+(2*4)+(1*0)=104
104 % 10 = 4
So 3937-40-4 is a valid CAS Registry Number.

3937-40-4SDS

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 arsine sulfide

1.2 Other means of identification

Product number -
Other names anilino-triphenyl-arsonium betaine

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:3937-40-4 SDS

3937-40-4Relevant academic research and scientific papers

Anthracene as a Launchpad for a Phosphinidene Sulfide and for Generation of a Phosphorus-Sulfur Material Having the Composition P2S, a Vulcanized Red Phosphorus That Is Yellow

Transue, Wesley J.,Nava, Matthew,Terban, Maxwell W.,Yang, Jing,Greenberg, Matthew W.,Wu, Gang,Foreman, Elizabeth S.,Mustoe, Chantal L.,Kennepohl, Pierre,Owen, Jonathan S.,Billinge, Simon J. L.,Kulik, Heather J.,Cummins, Christopher C.

, p. 431 - 440 (2019)

Thermolysis of a pair of dibenzo-7-phosphanorbornadiene compounds is shown to lead to differing behaviors: phosphinidene sulfide release and formation of amorphous P2S. These compounds, tBuP(S)A (1, A = C14H10 o

ATOM TRANSFER AND EXCHANGE REACTIONS INVOLVING OXYGEN, SULFUR AND SELENIUM

Baechler, Raymond D.,Stack, Mary,Stevenson, Karen,Vanvalkenburgh, Virginia

, p. 49 - 52 (2007/10/02)

A systematic comparison has been made of the reaction conditions required to bring about the thermal transfer or exchange of Group 16 terminal elements between Group 15 molecular centers.Where reaction conditions were suitable, kinetic analyses have been performed, with the observed second-order behavior supporting the presumed bimolecular character of these reactions.

PREPARATION OF TERTIARY ARSINE SULPHIDES. CRYSTAL AND MOLECULAR STRUCTURES OF THE ADDUCT OF AsMePh2S AND P(NMe2)3O

Brown, Douglas H.,Cameron, A. Forbes,Cross, Ronald J.,McLaren, Mary

, p. 1459 - 1462 (2007/10/02)

Several tertiary arsine sulphides have been prepared by the action of sulphur on tertiary arsines in C6H4Cl2-o at high temperatures.AsPh3 and AsMePh2 react with S2Cl2 to produce AsPh3Cl2 and AsMePh2Cl2, respectively, and no tertiary arsine sulphide, contr

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