847900-41-8 Usage
Molecular structure
A D-mannolactone core with two benzyl groups and a 2,3-dimethoxybutan-2,3-diyl side chain attached.
Derivative
It is a derivative of mannose, a naturally occurring sugar.
Usage
Commonly used in organic synthesis, chemical research, chemical, and pharmaceutical industries, as well as in academic research.
Complexity
It is a complex chemical compound, which requires careful handling and expertise when working with it.
Reactivity
Potential reactivity may pose risks, so proper safety precautions and knowledge are necessary when handling the compound.
Check Digit Verification of cas no
The CAS Registry Mumber 847900-41-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,9,0 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 847900-41:
(8*8)+(7*4)+(6*7)+(5*9)+(4*0)+(3*0)+(2*4)+(1*1)=188
188 % 10 = 8
So 847900-41-8 is a valid CAS Registry Number.
847900-41-8Relevant academic research and scientific papers
An efficient synthesis of β-C-glycosides based on the conformational restriction strategy: Lewis acid promoted silane reduction of the anomeric position with complete stereoselectivity
Terauchi, Masaru,Abe, Hiroshi,Matsuda, Akira,Shuto, Satoshi
, p. 3751 - 3754 (2007/10/03)
(Chemical Equation Presented) The reduction of glyconolactols having an anomeric carbon substituent by Et3SiH/TMSOTf proceeded with complete stereoselectivity to produce the corresponding β-C-glycosides when the substrates were conformationally restricted in the 4C 1-chair form by a 3,4-O-cyclic diketal or a 4,6-O-benzylidene protecting group. Thus, the efficient construction of β-C-glycosides was achieved on the basis of the conformation restriction strategy.
