7473-41-8 Usage
Chemical structure
A pentofuranose ring with three benzoyl groups attached to the hydroxyl groups at positions 1, 3, and 5 of the sugar molecule.
Functionality
Often used in organic chemistry as a protecting group for the hydroxyl groups of sugars.
Synthesis
Serves as a precursor for the synthesis of other functionalized sugar derivatives.
Structure and reactivity
Its structure and reactivity make it a valuable tool for the modification and manipulation of complex sugar molecules in various chemical and biochemical applications.
Stability
Exhibits stability, which is beneficial for its use in laboratory research and chemical synthesis.
Ease of handling
Its stability and ease of handling make it a practical choice for use in laboratory research and chemical synthesis.
Applications
Utilized in the study and synthesis of complex sugar molecules, which can be found in various biological systems and have potential applications in pharmaceuticals, biochemistry, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 7473-41-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7473-41:
(6*7)+(5*4)+(4*7)+(3*3)+(2*4)+(1*1)=108
108 % 10 = 8
So 7473-41-8 is a valid CAS Registry Number.
7473-41-8Relevant academic research and scientific papers
Total synthesis of 2'-O-methyl-β-L-arabinosyluridine and reassignment the nucleoside from penicillium sp. as 2'-O-methyl-β-L-uridine
Shen, Chunyang,Ding, Haixin,Tao, Xueping,Yang, Ruchun,Bai, Jiang,Cao, Ban-Peng,Peng, Yi-Yuan,Xiao, Qiang
, p. 68 - 72 (2020/01/30)
In order to validate the structure of a rarely reported naturally occurring nucleoside isolated from the broth of Penicillium sp. (NO. 64), practical syntheses of 2′-O-methyl-β-L-arabinosyluridine, 2′-O-methyl-α-L-arabinosyluridine, and 2′-O-methyl-β-L-uridine were accomplished. Comparing their nuclear magnetic resonance (NMR) spectra and physical data, its structure was reassigned as 2′-O-methyl-β-L-uridine instead of former reported 2′-O-methyl-β-L-arabinosyluridine.
