Welcome to LookChem.com Sign In|Join Free
  • or
1-Formyl-4-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)semicarbazide is a complex organic compound with the molecular formula C25H24N4O8. It is a derivative of semicarbazide, featuring a formyl group at the 1-position and a 2,3,5-tri-O-benzoyl-β-D-ribofuranosyl moiety at the 4-position. 1-formyl-4-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)semicarbazide is significant in the field of organic synthesis and medicinal chemistry, particularly for the synthesis of nucleoside analogs, which are important in the development of antiviral and anticancer drugs. The benzoyl groups protect the ribose sugar, allowing for selective reactions at other sites within the molecule. Once the desired modifications are made, the benzoyl protecting groups can be removed to yield the final product. 1-formyl-4-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)semicarbazide's structure and reactivity make it a valuable intermediate in the synthesis of various biologically active molecules.

80049-52-1

Post Buying Request

80049-52-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

80049-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80049-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,0,4 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80049-52:
(7*8)+(6*0)+(5*0)+(4*4)+(3*9)+(2*5)+(1*2)=111
111 % 10 = 1
So 80049-52-1 is a valid CAS Registry Number.

80049-52-1Relevant academic research and scientific papers

Syntheses and Structure Assignments of Six Azolinone Ribonucleosides

Haines, David R.,Leonard, Nelson J.,Wiemer, David F.

, p. 474 - 482 (2007/10/02)

N-Ribosidation of a series of azolinones was achieved via silylation and SnCl4 catalysis.N-Ribosidation of 4-imidazolin-2-one gave 1-β-D-ribofuranosyl-4-imidazolin-2-one; of 1,2,4-triazolin-3-one gave 2- and 4-β-D-ribofuranosyl-1,2,4-triazolin-3-one, and 2,4-di-β-D-ribofuranosyl-1,2,4-triazolin-3-one; and of 2-tetrazolin-5-one gave 1-β-D-ribofuranosyl-2-tetrazolin-5-one and 1,4-di-β-D-ribofuranosyl-2-tetrazolin-5-one.Structure assignments were based on NMR and mass spectra, microanalytical data, and interconversions.The triazolinone monoriboside isomer structures were differentiated by 13C NMR long-range coupling patterns, and the assignments were confirmed by X-ray crystallography.New syntheses were developed for several of the ribonucleosides by fashioning the azolinone rings from 2,3,5-tri-O-benzoylribofuranosyl isocyanate.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 80049-52-1