790662-12-3 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 10 carbon (C) atoms, 16 hydrogen (H) atoms, and 6 oxygen (O) atoms.
Explanation
The IUPAC name is a standardized nomenclature system used to uniquely identify chemical compounds. It provides information about the structure and stereochemistry of the molecule.
Explanation
Levocarnitine is a naturally occurring substance in the human body that plays a role in the metabolism of fats. This compound is a derivative of levocarnitine, meaning it has a similar structure but with some modifications.
Explanation
The stereochemistry of a molecule refers to the three-dimensional arrangement of its atoms. In this case, the compound has specific configurations at the 4th and 5th carbon atoms, which are designated as R (rectus) and S (sinister), respectively.
Explanation
The compound contains several functional groups, which are specific arrangements of atoms that determine its chemical properties. These include a dioxolane ring, carboxylic acid groups, an ester group, and methyl groups.
Explanation
Due to its structure and properties, this compound is used in the pharmaceutical industry for the treatment of various metabolic and genetic disorders. It may help improve the body's ability to metabolize fats and produce energy.
Explanation
The compound's role in fat metabolism and energy production makes it a candidate for use in sports nutrition and weight loss products. It may help enhance athletic performance and support weight management.
Explanation
The compound's properties make it a valuable ingredient in the development of drugs and supplements that target metabolic and energy-related conditions, such as fatigue, muscle weakness, and cardiovascular health.
Stereochemistry
(4R,5S)-rel
Functional Groups
Dioxolane, carboxylic acid, ester, and methyl groups
Pharmaceutical Applications
Treatment of metabolic and genetic disorders
Sports Nutrition and Weight Loss
Potential applications
Development of Drugs and Supplements
Targeting metabolic and energy-related conditions
Check Digit Verification of cas no
The CAS Registry Mumber 790662-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,0,6,6 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 790662-12:
(8*7)+(7*9)+(6*0)+(5*6)+(4*6)+(3*2)+(2*1)+(1*2)=183
183 % 10 = 3
So 790662-12-3 is a valid CAS Registry Number.
790662-12-3Relevant articles and documents
Synthesis of potassium 2,3,4-trihydroxy-2-methylbutanoate: A leaf-closing substance of Leucaena leucocephalam
Gogoi, Sanjib,Argade, Narshinha P.
, p. 9093 - 9097 (2004)
Starting from citraconic anhydride (2), a six step synthesis of leaf closing substance (±)-erythro potassium 2,3,4-trihydroxy-2-methyl- butanoate (1) has been described with 29% overall yield via diesterification, OsO4-dihydroxylation, acetonide protection, regioselective mono hydrolysis of unhindered ester moiety, borane-dimethylsulfide induced chemoselective reduction of carboxylic group and hydrolysis pathway. Surprisingly, the sodium borohydride reduction of monoester 5 and lithium borohydride reduction of 11 furnished the undesired regioisomer 7.
