515-25-3 Usage
Description
BETONICINE is an amino-acid betaine that is a trans-4-hydroxy-L-proline zwitterion, in which both of the hydrogens attached to the nitrogen have been replaced by methyl groups.
Uses
Used in Pharmaceutical Industry:
BETONICINE is used as a pharmaceutical compound for its potential therapeutic applications. Its unique structure and properties may contribute to various medicinal uses, such as targeting specific biological pathways or serving as a building block for drug development.
Used in Research and Development:
In the field of research and development, BETONICINE can be utilized as a key component in the synthesis of novel compounds or as a subject of study to understand its biological effects and potential applications in medicine and other industries.
Used in Chemical Synthesis:
As a chemical compound, BETONICINE can be employed in the synthesis of other complex molecules or materials, potentially leading to the creation of new products with specific properties and applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 515-25-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 515-25:
(5*5)+(4*1)+(3*5)+(2*2)+(1*5)=53
53 % 10 = 3
So 515-25-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO3/c1-8(2)4-5(9)3-6(8)7(10)11/h5-6,9H,3-4H2,1-2H3/t5-,6+/m1/s1
515-25-3Relevant articles and documents
Characterization of amino acid-derived betaines by electrospray ionization tandem mass spectrometry
Naresh Chary,Dinesh Kumar, Ch.,Vairamani,Prabhakar
experimental part, p. 79 - 88 (2012/05/04)
Betaines belong to the naturally occurring osmoprotectants or compatible solutes present in a variety of plants, animals and microorganisms. In recent years, metabolomic techniques have been emerging as a fundamental tool for biologists because the constellation of these molecules and their relative proportions provide with information about the actual biochemical condition of a biological system. Therefore, identification and characterization of biologically important betaines are crucial, especially for metabolomic studies. Most of the natural betaines are derived from amino acids and related homologues. Although, theoretically, all the amino acids can be converted to corresponding betaines by simple methylation of the amine group, only a few of the amino acid-derived betaines were fully characterized in the literature. Here, we report a combined electrospray ionization tandem and high-resolution mass spectrometry study of all the betaines derived from amino acids, including the isomeric betaines. The decomposition pathway of protonated, sodiated and potassiated molecule ions that enable unambiguous characterization of the betaines including the isomeric betaines and overlapping ionic species of different betaines is distinctive. Copyright
