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2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl fluoride is a complex organic compound with the molecular formula C28H21FO8. It is a derivative of α-D-arabinofuranosyl fluoride, where three hydroxyl groups at the 2, 3, and 5 positions are substituted with benzoyl groups. 2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl fluoride is primarily used as a protecting group in the synthesis of nucleoside analogs, which are important in the development of antiviral and anticancer drugs. The benzoyl groups protect the hydroxyl groups from unwanted reactions during the synthesis process, and can be removed later to yield the desired nucleoside product. The compound is also known for its stability and reactivity, making it a valuable intermediate in organic synthesis.

3862-86-0

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3862-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3862-86-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,6 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3862-86:
(6*3)+(5*8)+(4*6)+(3*2)+(2*8)+(1*6)=110
110 % 10 = 0
So 3862-86-0 is a valid CAS Registry Number.

3862-86-0Relevant academic research and scientific papers

Glycosyl fluorides from n-pentenyl-related glycosyl donors-application to glycosylation strategies

Fraser-Reid, Bert,Lopez, J. Cristobal,Bernal-Albert, Paloma,Gomez, Ana M.,Uriel, Clara,Ventura, Juan

, p. 51 - 65 (2013/03/28)

n-Pentenyl glycosides (NPGs) and n-pentenyl orthoesters (NPOEs) have been transformed into glycosyl fluorides by a variety of methods. In the case of NPGs, Barluenga's reagent, bis(pyridinium)iodonium(I)tetrafluoroborate (IPy 2BF4),

Reaction of 1,2-orthoesters with HF-pyridine: A method for the preparation of partly unprotected glycosyl fluorides and their use in saccharide synthesis

Cristobal Lopez,Ventura, Juan,Uriel, Clara,Gomez, Ana M.,Fraser-Reld, Bert

supporting information; experimental part, p. 4128 - 4131 (2009/12/30)

Glycosyl fluorides can be prepared In an efficient manner by treatment of pyranose- or furanose-derlved 1,2-orthoesters, with hydrogen fluoride pyridine (HF-py). The method Is compatible with the presence of a variety of protecting groups, including fert-

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