71662-16-3 Usage
Uses
Used in Biological Research:
a-D-Glucopyranose, 1-(dihydrogen phosphate), barium salt(1:1) is used as a research compound for studying the role of glucose and phosphate ions in cellular metabolism and their interactions with barium.
Used in Chemical Synthesis:
a-D-Glucopyranose, 1-(dihydrogen phosphate), barium salt(1:1) is used as a starting material or intermediate in the synthesis of various chemical products, particularly those involving glucose or phosphate derivatives.
Used in Medical Applications:
a-D-Glucopyranose, 1-(dihydrogen phosphate), barium salt(1:1) is used as a diagnostic or therapeutic agent in medical research, potentially aiding in the understanding or treatment of certain conditions related to glucose or phosphate metabolism.
Used in Industrial Processes:
a-D-Glucopyranose, 1-(dihydrogen phosphate), barium salt(1:1) may be employed in specific industrial processes where the unique properties of the glucose, phosphate, and barium combination are advantageous, such as in the development of new materials or catalysts.
Check Digit Verification of cas no
The CAS Registry Mumber 71662-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,6 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71662-16:
(7*7)+(6*1)+(5*6)+(4*6)+(3*2)+(2*1)+(1*6)=123
123 % 10 = 3
So 71662-16-3 is a valid CAS Registry Number.
71662-16-3Relevant articles and documents
Protecting-group-free synthesis of glycosyl 1-phosphates
Edgar, Landon John G.,Dasgupta, Somnath,Nitz, Mark
supporting information; experimental part, p. 4226 - 4229 (2012/09/22)
Glycosyl 1-phosphates enriched in the α-anomer are obtained without the use of protecting groups in two steps starting from the free hemiacetal. Condensation of free hemiacetals with toluenesulfonylhydrazide yields a range of glycosylsulfonohydrazide donors which can be oxidized using cupric chloride in the presence of phosphoric acid and the coordinating additive 2-methyl-2-oxazoline to give useful yields of the fully deprotected glycosyl 1-phosphates.
