183182-08-3 Usage
Uses
Used in Pharmaceutical Industry:
Lysine is used as a therapeutic agent for [application reason], such as promoting tissue growth, maintenance, and repair. Its role in protein synthesis makes it a valuable component in the development of medications targeting various health conditions.
Used in Nutritional Supplements:
Lysine is used as a dietary supplement to support [application reason], including the enhancement of immune function and the promotion of healthy brain function. As an essential amino acid, it is particularly important for individuals who may not receive adequate amounts through their diet.
Used in Cosmetics Industry:
Lysine is used as an ingredient in the cosmetics industry for [application reason], such as promoting skin health and collagen production. Its role in collagen synthesis makes it a valuable component in anti-aging and skin care products.
Used in Food Industry:
Lysine is used as an additive in the food industry to enhance [application reason], such as improving the nutritional value of certain products and supporting the body's protein requirements.
Used in Research and Development:
Lysine is used as a research compound for [application reason], including the study of its potential benefits in various physiological processes and the development of new therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 183182-08-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,1,8 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 183182-08:
(8*1)+(7*8)+(6*3)+(5*1)+(4*8)+(3*2)+(2*0)+(1*8)=133
133 % 10 = 3
So 183182-08-3 is a valid CAS Registry Number.
183182-08-3Relevant academic research and scientific papers
Catalytic Asymmetric Synthesis of Unprotected β2-Amino Acids
Zhu, Chendan,Mandrelli, Francesca,Zhou, Hui,Maji, Rajat,List, Benjamin
, p. 3312 - 3317 (2021/04/07)
We report here a scalable, catalytic one-pot approach to enantiopure and unmodified β2-amino acids. A newly developed confined imidodiphosphorimidate (IDPi) catalyzes a broadly applicable reaction of diverse bis-silyl ketene acetals with a silylated aminomethyl ether, followed by hydrolytic workup, to give free β2-amino acids in high yields, purity, and enantioselectivity. Importantly, both aromatic and aliphatic β2-amino acids can be obtained using this method. Mechanistic studies are consistent with the aminomethylation to proceed via silylium-based asymmetric counteranion-directed catalysis (Si-ACDC) and a transition state to explain the enantioselectivity is suggested on the basis of density functional theory calculation.
Enantioselective synthesis of β-amino acids. 7. Preparation of enantiopure α-substituted β-amino acids from 1-benzoyl-2(S)-tert-butyl-3-methylperhydropyrimidin-4-one
Juaristi, Eusebio,Quintana, Delia,Balderas, Margarita,Garcia-Perez, Enrique
, p. 2233 - 2246 (2007/10/03)
Inexpensive natural α-amino acid L-asparagine was efficiently converted to either (R)- or (S)-α-alkylated β-amino acids in enantiomerically pure state. The key intermediate in this protocol is the enantiopure N,N-acetal pyrimidinone (S)-1, a masked chiral derivative of β-alanine.
