2922-61-4 Usage
General Description
Pyruvic acid lithium salt is a chemical compound used in various biochemical and pharmaceutical applications. It is the lithium salt of pyruvic acid, a key intermediate in the glycolysis pathway and a precursor for the synthesis of amino acids and other metabolites. Pyruvic acid lithium salt is often used in cell culture media to support cell growth and metabolism. It can also be used as a source of energy in certain cell types and as a buffering agent in biological and chemical research. Additionally, it has been investigated for potential therapeutic use in conditions such as cancer, diabetes, and neurological disorders. Overall, pyruvic acid lithium salt is a versatile compound with diverse applications in research and medical fields.
Check Digit Verification of cas no
The CAS Registry Mumber 2922-61-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,2 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2922-61:
(6*2)+(5*9)+(4*2)+(3*2)+(2*6)+(1*1)=84
84 % 10 = 4
So 2922-61-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H4O3.Li/c1-2(4)3(5)6;/h1H3,(H,5,6);/q;+1/p-1
2922-61-4Relevant articles and documents
Complete conversion of l-lactate into d-lactate. A generic approach involving enzymatic catalysis, electrochemical oxidation of NADH, and electrochemical reduction of pyruvate
Biade, Azz-Eddine,Bourdillon, Christian,Laval, Jean-Marc,Mairesse, Gilles,Moiroux, Jacques
, p. 893 - 897 (2007/10/02)
L-Lactate was converted into D-lactate with a yield better than 97%, the system involving stereospecific catalysis of L-lactate oxidation by the rather cheap L-lactate dehydrogenase plus electrochemical regeneration of NAD+ at the anode and electrochemical reduction of pyruvate at the cathode. Such an approach can be extended to mere deracemization or complete inversion of all types of chiral α-alcohol-acids provided that the dehydrogenase related to the isomer to be inverted is available. Efficiency was not limited by enzyme or coenzyme deactivations.
