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(2-methoxyphenyl)arsonic acid is a chemical compound with the molecular formula C7H9AsO4. It is a derivative of arsenic and has a phenyl group with a methoxy substituent attached to the arsenic atom. (2-methoxyphenyl)arsonic acid is highly toxic and exposure to it can lead to serious health effects, such as liver and kidney damage, as well as neurological and developmental problems.

49784-54-5

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49784-54-5 Usage

Uses

Used in Agriculture:
(2-methoxyphenyl)arsonic acid is used as a herbicide and insecticide for controlling pests and unwanted plants in agricultural settings. Its effectiveness in controlling pests and plants is due to its toxic nature.
Used in Veterinary Medicine:
(2-methoxyphenyl)arsonic acid is used in the treatment of parasitic infections in animals. Its toxicity helps in eliminating parasites and improving the health of the animals.
However, due to its toxicity and potential environmental and health risks, the use of (2-methoxyphenyl)arsonic acid has been restricted or banned in many countries. Strict safety precautions should be taken when handling this chemical to minimize exposure and potential harm.

Check Digit Verification of cas no

The CAS Registry Mumber 49784-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,7,8 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 49784-54:
(7*4)+(6*9)+(5*7)+(4*8)+(3*4)+(2*5)+(1*4)=175
175 % 10 = 5
So 49784-54-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H9AsO4/c1-12-7-5-3-2-4-6(7)8(9,10)11/h2-5H,1H3,(H2,9,10,11)

49784-54-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methoxyphenyl)arsonic acid

1.2 Other means of identification

Product number -
Other names o-Methoxyphenylarsonsaeure

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:49784-54-5 SDS

49784-54-5Downstream Products

49784-54-5Relevant 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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