873660-49-2 Usage
Uses
Used in Medicinal Chemistry Research:
Butanoic acid, 2-hydroxy-4-(methylseleno)is used as a research compound for its potential therapeutic properties in the field of medicinal chemistry.
Used in Antioxidant Applications:
It is used as an antioxidant agent due to its ability to neutralize free radicals and protect cells from oxidative damage.
Used in Anti-inflammatory Applications:
Butanoic acid, 2-hydroxy-4-(methylseleno)is used as an anti-inflammatory agent for its potential to reduce inflammation and alleviate symptoms of inflammatory conditions.
Used in Anti-cancer Applications:
It is used as an anti-cancer agent for its potential to inhibit tumor growth and progression by modulating various oncological signaling pathways.
Used in Pharmaceutical Development:
Butanoic acid, 2-hydroxy-4-(methylseleno)is used as a key component in the development of novel pharmaceuticals and nutraceuticals due to its diverse pharmacological and biomedical applications.
Used in Selenium-related Disease Treatment:
It is used as a potential treatment for certain selenium-related diseases and conditions due to its selenium content and its potential to address selenium deficiency or toxicity.
Check Digit Verification of cas no
The CAS Registry Mumber 873660-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,6,6 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 873660-49:
(8*8)+(7*7)+(6*3)+(5*6)+(4*6)+(3*0)+(2*4)+(1*9)=202
202 % 10 = 2
So 873660-49-2 is a valid CAS Registry Number.
873660-49-2Relevant academic research and scientific papers
Preparation method of DL-hydroxy selenomethionine
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Paragraph 0020-0023, (2021/06/02)
The invention belongs to the field of preparation of organic compounds. The invention provides a preparation method of DL-hydroxy selenomethionine. The method is characterized in that gamma-butyrolactone is used as a raw material, alpha-hydroxyl-gamma-butyrolactone is synthesized through alpha-bromination and hydroxylation, and then the alpha-hydroxyl-gamma-butyrolactone reacts with sodium methyl selenol to obtain the DL-hydroxyl selenomethionine. The method has the advantages of easily available raw materials, mild reaction conditions and low cost, and is suitable for large-scale preparation of DL-hydroxyselenomethionine.
Process for preparing 2-hydroxy-4-methylselenobutyric acid, alone or as a mixture with its sulphur-containing analogue, and uses thereof in nutrition, in particular animal nutrition
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Page/Page column 7, (2012/12/13)
The present invention relates to a novel process for preparing 2-hydroxy-4-methylselenobutyric acid from 3-methylselenoproprion-aldehyde. The 2-hydroxy-4-methylselenobutyric acid is obtained alone or as a mixture with its sulphur-containing analogue. The invention also relates to the compositions, in particular nutritional compositions, comprising a mixture of 2-hydroxy-4-methylselenobutyric acid and 2-hydroxy-4-methylthiobutyric acid, and a physiologically acceptable medium, and to the use of this mixture as a dietary ingredient.
