52918-59-9 Usage
Uses
Used in Organic Synthesis:
2,3,4,5-tetra-O-acetyl-1,6-di-O-tritylhexitol is used as a building block for the synthesis of complex organic molecules. Its versatile structure allows for the creation of a wide range of compounds with potential applications in various industries.
Used in Carbohydrate Chemistry:
2,3,4,5-tetra-O-acetyl-1,6-di-O-tritylhexitol is used as a protecting group for hydroxyl groups in carbohydrate chemistry. This helps in the selective protection and deprotection of hydroxyl groups during the synthesis of complex carbohydrate structures.
Used in Pharmaceutical Industry:
2,3,4,5-tetra-O-acetyl-1,6-di-O-tritylhexitol is used as a key intermediate in the synthesis of various pharmaceuticals and biologically active compounds. Its unique structure and functional groups make it a valuable component in the development of new drugs and therapeutic agents.
Used in Biological Research:
2,3,4,5-tetra-O-acetyl-1,6-di-O-tritylhexitol is used as a starting material for the preparation of various biologically active compounds. Its presence in the synthesis of complex molecules can provide insights into the structure-function relationships of these compounds and their potential applications in biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 52918-59-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,9,1 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52918-59:
(7*5)+(6*2)+(5*9)+(4*1)+(3*8)+(2*5)+(1*9)=139
139 % 10 = 9
So 52918-59-9 is a valid CAS Registry Number.
52918-59-9Relevant academic research and scientific papers
2,3,4,5-tetra-?-acetyl-1,6-di-?-(triphenylmethyl)-D- mannitol
Shalaby, M. Ashraf,Fronczek, Frank R.,Voll, Ronald J.,Watkins, Steven F.,Younathan, Ezzat S.
, p. 381 - 383 (2007/10/03)
The central six-C-atom chain of the title compound, C52H50O10, adopts a nearly planar extended conformation free from C//C, C//O and O//O 1,3-parallel interactions. The three torsion angles formed by these atoms have values of 177.4(2), 174.2(2) and -178.0(2)°. The bulky triphenylmethyl groups, which are oriented gauche to their neighboring acetoxy groups with O-C-C-O torsion angles of -69.8 (2) and -63.0 (2)°, cause no distortion of the bond lengths and bond angles of the sugar moiety.
