228115-41-1 Usage
Uses
Used in Medicinal Chemistry:
.beta.-D-Gulopyranose, 1,6-anhydro-3-deoxy-3-(1,1-dimethylethoxy)carbonylaminois used as a building block in the synthesis of complex molecules for medicinal chemistry. Its unique structure allows for the development of novel compounds with potential therapeutic applications.
Used in Drug Development:
In the pharmaceutical industry, .beta.-D-Gulopyranose, 1,6-anhydro-3-deoxy-3-(1,1-dimethylethoxy)carbonylamino- is used as a key intermediate in the development of new drugs. Its distinctive features may contribute to the creation of innovative medications with improved efficacy and selectivity.
Used in Organic Synthesis:
.beta.-D-Gulopyranose, 1,6-anhydro-3-deoxy-3-(1,1-dimethylethoxy)carbonylaminois utilized as a synthetic building block in organic chemistry. It can be employed to construct a variety of organic compounds, expanding the scope of chemical research and development.
Used in Chemical Research:
.beta.-D-Gulopyranose, 1,6-anhydro-3-deoxy-3-(1,1-dimethylethoxy)carbonylaminoserves as a valuable research tool in chemical laboratories, where it can be used to study the properties and reactivity of carbohydrates and glycosides. Its unique structure may provide insights into the development of new synthetic methods and the understanding of biological processes involving these types of molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 228115-41-1 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, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 228115-41:
(8*2)+(7*2)+(6*8)+(5*1)+(4*1)+(3*5)+(2*4)+(1*1)=111
111 % 10 = 1
So 228115-41-1 is a valid CAS Registry Number.
228115-41-1Relevant 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
