61367-40-6 Usage
Uses
Used in Pharmaceutical Industry:
H-D-CHG-OH HCL is used as an active pharmaceutical ingredient for its potential therapeutic effects. H-D-CHG-OH HCL may be utilized in the development of drugs targeting various health conditions due to its role in physiological processes and the potential modifications provided by the addition of hydrochloric acid.
Used in Biochemical Research:
H-D-CHG-OH HCL is used as a research tool in biochemical studies to investigate the role of choline and its derivatives in cellular processes. H-D-CHG-OH HCL may be employed in experiments to understand the mechanisms of action and potential applications in biological systems.
Used in Industrial Applications:
H-D-CHG-OH HCL may be used in various industrial applications, such as the development of new materials or processes, due to its potential modifications in solubility, stability, or reactivity. H-D-CHG-OH HCL's properties may be harnessed to improve or create innovative products and technologies in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 61367-40-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,6 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61367-40:
(7*6)+(6*1)+(5*3)+(4*6)+(3*7)+(2*4)+(1*0)=116
116 % 10 = 6
So 61367-40-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO2.ClH/c10-8(11)6-9-7-4-2-1-3-5-7;/h7,9H,1-6H2,(H,10,11);1H
61367-40-6Relevant academic research and scientific papers
Nian, Yong,Wang, Jiang,Zhou, Shengbin,Wang, Shuni,Moriwaki, Hiroki,Kawashima, Aki,Soloshonok, Vadim A.,Liu, Hong
, p. 12918 - 12922 (2015)
Structurally simple and inexpensive chiral tridentate ligands were employed for substantially advancing the purely chemical dynamic kinetic resolution (DKR) of unprotected racemic tailor-made α-amino acids (TM-α-AAs), enabling the first DKR of TM-α-AAs bearing tertiary alkyl chains as well as multiple unprotected functional groups. Owing to the operationally convenient conditions, virtually complete stereoselectivity, and full recyclability of the source of chirality, this method should find wide applications for the preparation of TM-α-AAs, especially on large scale. The non-enzymatic dynamic kinetic resolution of racemic α-amino acids bearing tertiary alkyl chains and multiple unprotected functional groups is based on the enantioselective formation of nickel(II) complexes and their hydrolysis under convenient conditions. The specially designed chiral ligands are inexpensive and can be quantitatively recycled.
