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(3-methoxyphenyl)arsonic acid, also known as MPAA, is an organoarsenic compound with the molecular formula C7H9AsO4. It is structurally similar to phenylarsonic acid and has been used as a ligand in coordination complexes and as a reagent in organic synthesis. MPAA is also being studied for its potential use in treating parasitic infections. However, it is considered toxic and carcinogenic, and proper safety precautions should be taken when handling and using this chemical.

7400-88-6

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7400-88-6 Usage

Uses

Used in Chemical Synthesis Industry:
(3-methoxyphenyl)arsonic acid is used as a reagent for [application reason] in the chemical synthesis industry.
Used in Coordination Chemistry:
(3-methoxyphenyl)arsonic acid is used as a ligand for [application reason] in the synthesis of coordination complexes.
Used in Pharmaceutical Research:
(3-methoxyphenyl)arsonic acid is used as a potential treatment for [application reason] in the research of parasitic infections.
Note: The specific application reasons are not provided in the materials, so they are left blank.

Check Digit Verification of cas no

The CAS Registry Mumber 7400-88-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,0 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7400-88:
(6*7)+(5*4)+(4*0)+(3*0)+(2*8)+(1*8)=86
86 % 10 = 6
So 7400-88-6 is a valid CAS Registry Number.

7400-88-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methoxyphenyl)arsonic acid

1.2 Other means of identification

Product number -
Other names (3-Methoxy-phenyl)-arsonsaeure

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:7400-88-6 SDS

7400-88-6Relevant academic research and scientific papers

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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