83833-15-2 Usage
Description
Beta-d-Glucopyranose, 1-(dihydrogen phosphate), disodium salt is a chemical compound derived from glucose, which is a disodium salt of the dihydrogen phosphate ester of beta-d-Glucopyranose. It contains two sodium ions, a glucose molecule, and a phosphate group.
Uses
Used in Pharmaceutical and Food Industry:
Beta-d-Glucopyranose, 1-(dihydrogen phosphate), disodium salt is used as a buffering agent and a stabilizer in pharmaceuticals and food products to maintain the pH and stability of the products.
Used in Cell Culture Media:
It is used in cell culture media to provide essential nutrients and maintain the pH and stability of the media.
Used in Chemical and Biochemical Production:
Beta-d-Glucopyranose, 1-(dihydrogen phosphate), disodium salt is used in the production of various chemicals and biochemicals due to its ability to act as a phosphorylating agent.
Used in Organic Compound Synthesis:
It can be used in the synthesis of other organic compounds due to its ability to act as a phosphorylating agent, making it a versatile compound in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 83833-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,3 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83833-15:
(7*8)+(6*3)+(5*8)+(4*3)+(3*3)+(2*1)+(1*5)=142
142 % 10 = 2
So 83833-15-2 is a valid CAS Registry Number.
83833-15-2Relevant articles and documents
Synthesis and use of glycosyl phosphites: An effective route to glycosyl phosphates, sugar nucleotides, and glycosides
Sim, Mui Mui,Kondo, Hirosato,Wong, Chi-Huey
, p. 2260 - 2267 (2007/10/02)
An efficient and convenient synthetic route to glycosyl phosphites and phosphates has been developed that uses dibenzyl N,N-diethylphosphoramidite as a phosphitylating reagent. Glycosyl phosphites and phosphates of 2-acetamido-2-deoxy-D-galactose (GalNAc) (29), 2-acetamido-2-deoxy-D-glucose (GlcNAc) (30), D-galactose (Gal) (31), D-glucose (Glc) (32), D-mannose (Man) (33), L-rhamnose (Rha) (34), L-fucose (Fuc) (35), and N-acetylneuraminic acid (NeuAc) (41) were prepared by this procedure. Compounds 29 and 30 were obtained as α anomers exclusively, whereas compounds 31, 32, and 41 were obtained as β anomers, and compounds 33 and 34, as α anomers, predominately. The phosphates are useful for the synthesis of sugar nucleotides, and the phosphites are effective glycosylation reagents.
