103192-55-8 Usage
Description
D(+)-GLUCOPYRANOSE 6-PHOSPHATE MONOPOTASSIUM SALT is a chemical compound derived from glucose, featuring a D(+)-glucose molecule phosphorylated at the sixth carbon atom and bound to a potassium ion. It is known for its stability and solubility in aqueous solutions, making it a preferred form for experimental use.
Used in Biochemical and Biological Research:
D(+)-GLUCOPYRANOSE 6-PHOSPHATE MONOPOTASSIUM SALT is used as a substrate for enzymatic reactions and as a reagent in various laboratory assays. Its role in these applications is crucial for studying the mechanisms and kinetics of different biochemical processes.
Used in the Study of Glycolysis:
D(+)-GLUCOPYRANOSE 6-PHOSPHATE MONOPOTASSIUM SALT is used as a key intermediate in the process of glycolysis for understanding the metabolic pathway that breaks down glucose to produce energy. This application aids researchers in exploring the fundamentals of cellular respiration and energy production.
Check Digit Verification of cas no
The CAS Registry Mumber 103192-55-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,1,9 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103192-55:
(8*1)+(7*0)+(6*3)+(5*1)+(4*9)+(3*2)+(2*5)+(1*5)=88
88 % 10 = 8
So 103192-55-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H13O9P.K/c7-3-2(1-14-16(11,12)13)15-6(10)5(9)4(3)8;/h2-10H,1H2,(H2,11,12,13);
103192-55-8Relevant articles and documents
Analysis of the Chirality of 16O, 17O, 18O> Phosphate Esters by 31P Nuclear Magnetic Resonance Spectroscopy
Jarvest, Richard L.,Lowe, Gordon,Potter, Barry V. L.
, p. 3186 - 3195 (2007/10/02)
A stereospecific method for cyclising D-glucose 6-16O, 17O, 18O>phosphate and adenosine 5'-16O, 17O, 18O>-phosphate to their conformationally locked six-membered cyclic phosphate diesters has been developed.Using 16O, 17O, 18O>phosphate esters of known absolute configuration it is shown by 31P n.m.r. spectroscopy, after esterification to the axial and equatorial triesters, that the cyclisation occurs with inversion of configuration.It is now possible, therefore, to determine the chirality at phosphorus of D-glucose 6-16O, 17O, 18O>phosphate and adenosine 5'-16O, 17O, 18O>phosphate by this procedure.