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(2R,3R,4S,5S,6S)-2-(acetoxymethyl)-6-((4-chlorophenyl)amino)tetrahydro-2H-pyran-3,4,5-triyl triacetate is a complex organic compound with a molecular formula of C20H25ClO8. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific stereochemistry, with the R and S configurations at various carbon centers. (2R,3R,4S,5S,6S)-2-(acetoxymethyl)-6-((4-chlorophenyl)amino)tetrahydro-2H-pyran-3,4,5-triyl triacetate features a tetrahydro-2H-pyran ring, which is a type of cyclic ether, and is further functionalized with acetoxymethyl, (4-chlorophenyl)amino, and triacetate groups. The presence of the 4-chlorophenyl group suggests potential applications in pharmaceuticals or agrochemicals, as such structures can interact with biological targets. The compound's structure and functional groups may also imply its use in the synthesis of more complex molecules or as a precursor in organic chemistry.

2862-01-3

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2862-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2862-01-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,6 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2862-01:
(6*2)+(5*8)+(4*6)+(3*2)+(2*0)+(1*1)=83
83 % 10 = 3
So 2862-01-3 is a valid CAS Registry Number.

2862-01-3Downstream Products

2862-01-3Relevant academic research and scientific papers

Stereoselective copper-catalyzed Chan-Lam-Evans N-arylation of glucosamines with arylboronic acids at room temperature

Bruneau, Alexandre,Brion, Jean-Daniel,Alami, Mouad,Messaoudi, Samir

supporting information, p. 8359 - 8361 (2013/09/23)

An efficient and practical N-arylation of glycosylamines with substituted aryl boronic acids has been established. Using Cu(OAc)2 and pyridine at room temperature under air atmosphere, the protocol proved to be general, and a variety of aryl N-glycosides have been prepared in good to excellent yields with exclusive β selectivity.

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