873660-49-2 Usage
General Description
Butanoic acid, 2-hydroxy-4-(methylseleno)- is a organic compound that is a derivative of butanoic acid with a hydroxy group and a methylseleno group attached to the fourth carbon atom. It is a yellow oily liquid with a pungent, rancid odor. Butanoic acid, 2-hydroxy-4-(methylseleno)- is primarily used in research and experimental studies, particularly in the field of medicinal chemistry due to its potential therapeutic properties. It has been studied for its antioxidant, anti-inflammatory, and anti-cancer activities, and it also has potential applications in the development of novel pharmaceuticals and nutraceuticals. Moreover, it has also been investigated for its potential role in the treatment of certain selenium-related diseases and conditions. Overall, 2-hydroxy-4-(methylseleno)-butanoic acid is a compound of interest in the scientific community for its diverse pharmacological and biomedical applications.
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 articles and documents
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.
