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5410-28-6

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5410-28-6 Usage

Description

(2-iodophenyl)arsonic acid is an organoarsenic compound characterized by a phenyl ring with a carboxylic acid group and an arsenic atom attached through a double bond. It has a molecular formula of C6H6AsIO3 and a molecular weight of 314.90 g/mol. This solid compound at room temperature is soluble in organic solvents like ethanol and acetone. Due to potential health risks associated with exposure, handling it requires proper safety measures.

Uses

Used in Pharmaceutical Synthesis:
(2-iodophenyl)arsonic acid serves as an intermediate in the synthesis of pharmaceuticals, contributing to the development of various medicinal compounds.
Used in Organic Compounds Synthesis:
It is also utilized in the synthesis of other organic compounds, highlighting its versatility in chemical reactions and its potential applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 5410-28-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5410-28:
(6*5)+(5*4)+(4*1)+(3*0)+(2*2)+(1*8)=66
66 % 10 = 6
So 5410-28-6 is a valid CAS Registry Number.

5410-28-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-iodophenyl)arsonic acid

1.2 Other means of identification

Product number -
Other names o-iodophenylarsonic acid

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:5410-28-6 SDS

5410-28-6Relevant articles and documents

SYNTHESIS AND PROPERTIES OF ARYLARSONIC ACIDS

Yambushev, F. D.,Kovyrzina, V>,P.,Shagidullin, R. R.,Gorchakova, L. A.,Fedotov, B. G.,et al.

, p. 1919 - 1926 (2007/10/02)

1.A number of arylarsonic acids with various substituents in the ortho, meta, and para positions in the benzene ring were synthesized from diazonium salts by the Bart reaction; the products were characterized by their IR spectra. 2.By the DTA method it was established that arylarsonic acid molecules were linked together through hydrogen bonds to form oligomeric associated forms. 3.The IR spectra of arylarsonic acids confirm the presence in them of strong hydrogen bonds through which they are able to undergo association into two forms differing in the symmetry of the d isposition of the As=O bonds.A form which gives a C band arises if the arsonyl oxygen participates in the formation of two hydrogen bonds simultaneously, as a result of which the molecules are linked together to form endless chains and columns.In the other form there are probably cyclic dimers with intermolecular H bonds.

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