63301-57-5 Usage
Chemical structure
A complex chemical compound derived from a hexopyranose sugar molecule.
Functional groups
Contains four acetyl groups attached to carbon atoms in positions 1, 3, 4, and 6, and a sulfonyl amino group attached to the 2-deoxy carbon atom.
Applications
Potential use in medicinal chemistry, particularly in the development of new pharmaceutical drugs.
Research significance
Valuable tool for studying the structure and function of sugar molecules and for designing new molecules with specific biological activities.
Molecular weight
Approximately 499.55 g/mol (calculated from the molecular formula).
Solubility
Likely soluble in organic solvents such as methanol, ethanol, or acetone, due to the presence of acetyl groups.
Stability
Relatively stable under normal laboratory conditions, but sensitive to hydrolysis or deacetylation reactions.
Synthesis
Typically synthesized through a series of chemical reactions involving the protection of hydroxyl groups, introduction of the sulfonyl amino group, and subsequent acetylation.
Purity
Often characterized by techniques such as nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry to confirm its structure and purity.
Check Digit Verification of cas no
The CAS Registry Mumber 63301-57-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,0 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63301-57:
(7*6)+(6*3)+(5*3)+(4*0)+(3*1)+(2*5)+(1*7)=95
95 % 10 = 5
So 63301-57-5 is a valid CAS Registry Number.
63301-57-5Relevant articles and documents
Convenient stereocontrolled amidoglycosylation of alcohols with acetylated glycals and trichloroethoxysulfonamide
Murakami, Teiichi,Sato, Yukari,Yoshioka, Kyoko,Tanaka, Mutsuo
, p. 121 - 131 (2016/09/23)
A regio- and stereo-controlled, rhodium(II)-catalyzed amidoglycosylation of alcohols has been developed using O-acetylated glycals, trichloroethoxysulfonamide, and iodosobenzene. This one-pot amidoglycosylation was applied to a variety of primary and secondary alcohols to afford the β-O-glycosides with acceptable yields up to 84%. The reaction would proceed via stereoselective intermolecular aziridination of the glycal from the α-face followed by SN2 reaction with alcohol at C-1 from the β-face to give 1,2:2,3-di-trans-substituted isomer only.
