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(4-hydroxy-3-nitrophenyl)arsonous acid is an organoarsenic compound that contains both arsenic and phenol groups. It is structurally similar to arsenous acid and is highly toxic, posing significant health risks to humans and the environment.

5410-79-7

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5410-79-7 Usage

Uses

Used in Research and Development:
(4-hydroxy-3-nitrophenyl)arsonous acid is used as a chemical compound in research and development for its unique properties and potential applications in various fields. However, due to its high toxicity, it is handled with extreme care and its use is restricted.
Used in Chemical Analysis:
In chemical analysis, (4-hydroxy-3-nitrophenyl)arsonous acid may be used as a reagent or in the synthesis of other compounds. Its application is limited due to its toxicity, and it is essential to follow strict safety protocols when working with (4-hydroxy-3-nitrophenyl)arsonous acid.
Used in Environmental Monitoring:
(4-hydroxy-3-nitrophenyl)arsonous acid can be used in environmental monitoring to detect and measure the presence of arsenic and other toxic elements in the environment. This is crucial for assessing the potential health risks and implementing appropriate safety measures.

Check Digit Verification of cas no

The CAS Registry Mumber 5410-79-7 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, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5410-79:
(6*5)+(5*4)+(4*1)+(3*0)+(2*7)+(1*9)=77
77 % 10 = 7
So 5410-79-7 is a valid CAS Registry Number.

5410-79-7SDS

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 (4-hydroxy-3-nitrophenyl)arsonous acid

1.2 Other means of identification

Product number -
Other names -

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:5410-79-7 SDS

5410-79-7Upstream product

5410-79-7Downstream Products

5410-79-7Relevant academic research and scientific papers

CDK inhibitor based on organic arsine as well as preparation method and application of CDK inhibitor

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Paragraph 0439-0444, (2021/03/31)

The invention provides a CDK inhibitor based on organic arsine as well as a preparation method and application of the CDK inhibitor. Specifically, the invention providese compounds of Formula I, or stereoisomers or tautomers thereof, or pharmaceutically acceptable salts, hydrates or solvates thereof; and the invention also discloses a preparation method and application thereof. Definitions of allgroups in the formula are shown in the specification.

Methylated Phenylarsenical Metabolites Discovered in Chicken Liver

Peng, Hanyong,Hu, Bin,Liu, Qingqing,Li, Jinhua,Li, Xing-Fang,Zhang, Hongquan,Le, X. Chris

supporting information, p. 6773 - 6777 (2017/06/06)

We report the discovery of three toxicologically relevant methylated phenylarsenical metabolites in the liver of chickens fed 3-nitro-4-hydroxyphenylarsonic acid (ROX), a feed additive in poultry production that is still in use in several countries. Methyl-3-nitro-4-hydroxyphenylarsonic acid (methyl-ROX), methyl-3-amino-4-hydroxyphenylarsonic acid (methyl-3-AHPAA), and methyl-3-acetamido-4-hydroxyphenylarsonic acid (or methyl-N-acetyl-ROX, methyl-N-AHPAA) were identified in such chicken livers, and the concentration of methyl-ROX was as high as 90 μg kg?1, even after a five-day clearance period. The formation of these newly discovered methylated metabolites from reactions involving trivalent phenylarsonous acid substrates, S-adenosylmethionine, and the arsenic (+3 oxidation state) methyltransferase enzyme As3MT suggests that these compounds are formed by addition of a methyl group to a trivalent phenylarsenical substrate in an enzymatic process. The IC50 values of the trivalent phenylarsenical compounds were 300–30 000 times lower than those of the pentavalent phenylarsenicals.

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