228115-91-1 Usage
Description
L-glycero-L-galacto-Heptitol, 2,6-anhydro-3,4,5-tris-O-(phenylmethyl)-, 1-(4-methylbenzenesulfonate) is a complex chemical compound that is a synthetic sugar alcohol derivative. It is commonly used in organic chemistry and biochemistry research. L-glycero-L-galacto-Heptitol, 2,6-anhydro-3,4,5-tris-O-(phenylmethyl)-, 1-(4-methylbenzenesulfonate) features three phenylmethyl groups attached to the sugar molecule, making it a valuable protective group in the synthesis of complex carbohydrates. Additionally, the 4-methylbenzenesulfonate group serves as a common leaving group in chemical reactions, which is beneficial for the formation of glycosidic linkages. As a result, this compound is instrumental in the field of organic chemistry, particularly in the synthesis and study of complex carbohydrates.
Uses
Used in Organic Chemistry Research:
L-glycero-L-galacto-Heptitol, 2,6-anhydro-3,4,5-tris-O-(phenylmethyl)-, 1-(4-methylbenzenesulfonate) is used as a protective group for the synthesis of complex carbohydrates. Its phenylmethyl groups provide a stable and easily removable protective layer during the synthesis process, which is crucial for the successful construction of intricate carbohydrate structures.
Used in Biochemistry Research:
In biochemistry, L-glycero-L-galacto-Heptitol, 2,6-anhydro-3,4,5-tris-O-(phenylmethyl)-, 1-(4-methylbenzenesulfonate) is employed for the study of carbohydrate structures and their interactions with biological molecules. L-glycero-L-galacto-Heptitol, 2,6-anhydro-3,4,5-tris-O-(phenylmethyl)-, 1-(4-methylbenzenesulfonate)'s unique structure allows researchers to investigate the role of carbohydrates in various biological processes and their potential as therapeutic agents.
Used in the Synthesis of Glycosidic Linkages:
L-glycero-L-galacto-Heptitol, 2,6-anhydro-3,4,5-tris-O-(phenylmethyl)-, 1-(4-methylbenzenesulfonate) is used as a key intermediate in the formation of glycosidic linkages. The 4-methylbenzenesulfonate group acts as a leaving group, facilitating the coupling of carbohydrate units to form larger, more complex structures. This is particularly important in the development of new glycoconjugates and glycoproteins with potential applications in medicine and biotechnology.
Check Digit Verification of cas no
The CAS Registry Mumber 228115-91-1 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, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 228115-91:
(8*2)+(7*2)+(6*8)+(5*1)+(4*1)+(3*5)+(2*9)+(1*1)=121
121 % 10 = 1
So 228115-91-1 is a valid CAS Registry Number.
228115-91-1Relevant articles and documents
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 (1999)
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
