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Arsenotrithious acid triphenyl ester, also known as triphenyl arsonous acid, is a chemical compound with the formula (C6H5)3AsOAs(OH)2. It is a derivative of arsonous acid, where three phenyl groups are attached to the arsenic atom. arsenotrithious acid triphenyl ester is an organoarsenic compound, which means it contains carbon-arsenic bonds. It is typically synthesized by reacting triphenyl arsonium chloride with water or a base. Arsenotrithious acid triphenyl ester is a colorless solid and is sensitive to light and heat. It has been used in the past as an analytical reagent and in the synthesis of other organoarsenic compounds. Due to its potential toxicity and environmental concerns, its use has been limited, and it is important to handle arsenotrithious acid triphenyl ester with care, following proper safety protocols.

1776-70-1

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1776-70-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1776-70-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,7 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1776-70:
(6*1)+(5*7)+(4*7)+(3*6)+(2*7)+(1*0)=101
101 % 10 = 1
So 1776-70-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H15AsS3/c1-4-10-16(11-5-1)20-19(21-17-12-6-2-7-13-17)22-18-14-8-3-9-15-18/h1-15H

1776-70-1SDS

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 tris(phenylsulfanyl)arsane

1.2 Other means of identification

Product number -
Other names Arsenigsaeure-trithiophenylester

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:1776-70-1 SDS

1776-70-1Relevant academic research and scientific papers

Reactivity of the pentelidene complexes [Cp*E{W(CO)5}2] (E = P, As) towards dichalcogenides and chalcogenols - synthesis of novel chalcogenopentelidene complexes

Lassandro, Giuliano,Rummel, Lena,Scheer, Manfred,Seidl, Michael,Timoshkin, Alexey Y.

supporting information, p. 12648 - 12654 (2021/09/28)

Pentelidene complexes of the type [Cp*E{W(CO)5}2] (Cp* = C5Me5;1a: E = P,1b: E = As) were reacted with the dichalcogenides R2Ch2(R = Ph, Mes, Tipp; Ch = S, Se, Te; Mes = 2,4,6-trimethylphenyl; Tipp = 2,4,6-triisopropylphenyl) and the chalcogenols PhChH (Ch = S, Se). It has been shown that the formation of new E-Ch bonds proceeds under elimination of the Cp* substituent. The resulting chalcogenopentelidene complexes, which have been isolated and fully characterised, represent a novel class of phosphinidene complexes which can be synthesised through this general synthetic route.

Preparation of 2-picolylarsonic acid and its reductive cleavage by ascorbic acid/iodine and by thiophenol

Ioannou, Panayiotis V.,Afroudakis, Pantelis A.,Siskos, Michael G.

, p. 2773 - 2783 (2007/10/03)

Contrary to dialkylaminoethyl halides, 2-picolyl chloride reacts with alkaline arsenite to give nearly quantitative yields 2-picolylarsonic acid. This acid is decomposed by ascorbic acid in the presence of catalytic amounts of iodine to 2-picoline and arsenious acid, most likely by hydride transfer from the ascorbic acid. Thiophenol decomposes this arsonic acid very quickly to 2-picoline, diphenyl disulfide and triphenyl trithioarsenite. In this case a proton from the thiophenol is transferred to the incipient 2-picolyl carbanion.

REACTION OF ARSENIC(III) OXIDE, ARSENOUS AND ARSENIC ACIDS WITH THIOLS

Serves, Spyros V.,Charalambidis, Yiannis C.,Sotiropoulos, Demetrios N.,Ioannou, Panayiotis V.

, p. 109 - 116 (2007/10/03)

Arsenic(III) oxide and arsenous acid in water or aqueous ethanolic solutions react, at room temperature, with a variety of lipophilic and hydrophilic thiols giving quantitatively triaryl and trialkyl trithioarsenites, (ArS)3As and (RS)3As.Aqueous solution

A new method of synthesis of arsenic trithiophenoxide

Chaudhry, S C,Mahajan, R K,Bhatt, S S,Sharma, Neeraj

, p. 279 - 280 (2007/10/02)

Arsenic trithiophenoxide As(C6H5S)3, has been synthesized by a novel method using arsenious oxide and thiophenol.The product has been characterized on the basis of IR and mass spectrometry.

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