2480-26-4 Usage
Description
H-L-MESER-OH HCL, also known as N-methyl-L-serine hydrochloride, is a chemical compound derived from the amino acid serine. It possesses unique properties that make it suitable for various applications, particularly in the pharmaceutical and cosmetic industries.
Uses
Used in Pharmaceutical Industry:
H-L-MESER-OH HCL is used as an active pharmaceutical ingredient for the development of drugs targeting various medical conditions. Its specific application reason in this industry is due to its unique chemical structure and potential therapeutic effects.
Used in Cosmetic Industry:
H-L-MESER-OH HCL is used as a topical compound in anti-aging agents, cosmetic peptides, and skin-conditioning agents. The application reason is its ability to improve skin health and appearance by promoting collagen production and providing moisturizing and anti-aging benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 2480-26-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,8 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2480-26:
(6*2)+(5*4)+(4*8)+(3*0)+(2*2)+(1*6)=74
74 % 10 = 4
So 2480-26-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H9NO3/c1-5-3(2-6)4(7)8/h3,5-6H,2H2,1H3,(H,7,8)/t3-/m0/s1
2480-26-4Relevant articles and documents
General method for the synthesis of N-methyl amino acids and N-alkyl amino esters from O'Donnell's Schiff bases
Chruma, Jason J.,Sames, Dalibor,Polt, Robin
, p. 5085 - 5086 (1997)
N-methyl amino acids, including L-abrine, and N-alkyl amino esters, were synthesized by reductive amination of O'Donnell's Schiff base amino esters with NaBH3CN and formaldehyde, or the appropriate aldehyde in CH3CN or THF in good to excellent yields, and with high purity.
Domino 1,3-dipolar cycloadditions of n- alkyl-α-amino esters with paraformaldehyde: A direct access to α-hydroxymethyl α-amino acids
Castelló, Luis M.,Nájera, Carmen,Sansano, José M.
, p. 967 - 971 (2014/04/03)
N-Alkyl-α-amino esters undergo a domino reaction, based on the iminium cation generation, with paraformaldehyde, followed by a 1,3-dipolar cycloaddition of the stabilized azomethA?ine ylide with another equivalent of formaldehyde. The resulting products are oxazolidines, which can be transformed after hydrolysis into α-hydroxymethyl α-amino acid or its derivatives. The diastereoselective 1,3-dipolar cycloaddition was performed using sarcosine (-)-menthyl or (-)-8-phenylmenthyl esters affording the cyclic product with moderate enantiomeric ratio. Georg Thieme Verlag Stuttgart · New York.
