228115-53-5 Usage
Uses
Used in Pharmaceutical Development:
.beta.-D-Galactopyranose, 1,6-dideoxy-1,6-epithio-3,4-O-(1-methylethylidene)-, bis(phenylmethyl) phosphate is used as a potential candidate for the development of new anti-cancer or anti-viral drugs. Its unique chemical structure and potential biological activities make it a valuable compound for exploring novel therapeutic approaches.
Used in Laboratory Research:
In the field of laboratory research, .beta.-D-Galactopyranose, 1,6-dideoxy-1,6-epithio-3,4-O-(1-methylethylidene)-, bis(phenylmethyl) phosphate serves as a useful tool for studying carbohydrate chemistry and biochemistry. Its modified structure allows researchers to investigate the interactions and effects of such compounds on biological systems.
Used in Drug Delivery Systems:
.beta.-D-Galactopyranose, 1,6-dideoxy-1,6-epithio-3,4-O-(1-methylethylidene)-, bis(phenylmethyl) phosphate may also be employed in the development of drug delivery systems, where its unique structure could potentially enhance the delivery, bioavailability, and therapeutic outcomes of various pharmaceutical agents.
Used in Carbohydrate Chemistry and Biochemistry Research:
.beta.-D-Galactopyranose, 1,6-dideoxy-1,6-epithio-3,4-O-(1-methylethylidene)-, bis(phenylmethyl) phosphate is used as a research tool for studying the structure, function, and interactions of carbohydrates in biological systems. Its modified structure provides insights into the role of sugar molecules in various biological processes and their potential applications in drug development and therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 228115-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,8,1,1 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 228115-53:
(8*2)+(7*2)+(6*8)+(5*1)+(4*1)+(3*5)+(2*5)+(1*3)=115
115 % 10 = 5
So 228115-53-5 is a valid CAS Registry Number.
228115-53-5Relevant academic research and scientific papers
Synthesis studies of structural analogues of tagetitoxin: 4-O-acetyl-3- amino-1,6-anhydro-3-deoxy-D-gulose 2-phosphate
Dent, Barry R.,Furneaux, Richard H.,Gainsford, Graeme J.,Lynch, Gregory P.
, p. 6977 - 6996 (2007/10/03)
Synthetic approaches to structural analogues of tagetitoxin (1) are described. The successful route to analogue 3 (X=O) has, as a key step, protection of the cis-vicinal amino alcohol moiety of compound 7 as an N- benzylated cyclic carbamate (9). X-Ray cr
