201023-39-4 Usage
Uses
Used in Nutritional Supplements:
Phenylalanine, phenylalanylis used as a nutritional supplement to support protein synthesis and overall health. It helps in the maintenance of muscle mass and the production of essential neurotransmitters, which are crucial for mood regulation and stress response.
Used in Artificially Sweetened Products:
Phenylalanine, phenylalanylis used as an additive in some artificially sweetened products to enhance their taste and provide a protein source for individuals who may have dietary restrictions or preferences.
Used in Medical Applications for Phenylketonuria Management:
Phenylalanine, phenylalanylis monitored and managed in the diets of individuals with phenylketonuria, a genetic disorder that impairs the body's ability to process this amino acid. Specialized dietary plans and medical interventions are employed to ensure that phenylalanine levels are maintained within a safe range, preventing the accumulation of toxic metabolites and associated neurological complications.
Used in Research and Development:
Phenylalanine, phenylalanylis utilized in research and development for the study of protein synthesis, neurotransmitter production, and the understanding of phenylketonuria. This amino acid serves as a valuable tool for scientists to explore the mechanisms of amino acid metabolism and develop potential therapeutic interventions for related disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 201023-39-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,0,2 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 201023-39:
(8*2)+(7*0)+(6*1)+(5*0)+(4*2)+(3*3)+(2*3)+(1*9)=54
54 % 10 = 4
So 201023-39-4 is a valid CAS Registry Number.
201023-39-4Relevant academic research and scientific papers
Biomimetic protecting-group-free 2′, 3′-selective aminoacylation of nucleosides and nucleotides
Her, Sohyoung,Kluger, Ronald
supporting information; experimental part, p. 676 - 678 (2011/03/22)
Aminoacyl phosphate monoesters can be prepared free of an amino-protecting group and used directly in lanthanum-promoted selective monoacylation of either the 2′ or 3′-hydroxyl of nucleosides and nucleotides. For example, phenylalanyl ethyl phosphate rapi
