228115-86-4 Usage
Uses
Used in Pharmaceutical Industry:
L-glycero-L-galacto-Heptitol, 2,6-anhydro-3,4-O-(1-methylethylidene)-, 1,7-bis(4-methylbenzenesulfonate) is used as a pharmaceutical intermediate for the development of drugs targeting conditions such as diabetes and obesity. Its unique structure and properties make it a promising candidate for creating novel therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, L-glycero-L-galacto-Heptitol, 2,6-anhydro-3,4-O-(1-methylethylidene)-, 1,7-bis(4-methylbenzenesulfonate) serves as a key building block for the synthesis of complex organic molecules. Its versatile chemical properties allow it to be incorporated into a wide range of compounds, expanding the scope of synthetic chemistry.
Used in Specialty Chemicals Production:
L-glycero-L-galacto-Heptitol, 2,6-anhydro-3,4-O-(1-methylethylidene)-, 1,7-bis(4-methylbenzenesulfonate) is also utilized in the production of specialty chemicals, where its unique properties can be harnessed to create high-value products for various applications. Its synthesis and use in this context require expert knowledge and careful handling to ensure safety and effectiveness.
Check Digit Verification of cas no
The CAS Registry Mumber 228115-86-4 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, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 228115-86:
(8*2)+(7*2)+(6*8)+(5*1)+(4*1)+(3*5)+(2*8)+(1*6)=124
124 % 10 = 4
So 228115-86-4 is a valid CAS Registry Number.
228115-86-4Relevant 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
