Welcome to LookChem.com Sign In|Join Free
  • or
The chemical compound "(3aS)-3c-hydroxy-2t-hydroxymethyl-(3ar,9ac)-2,3,3a,9a-tetrahydro-furo[2',3':4,5]oxazolo[3,2-c]pyrimidine-6,8-dione" is a complex organic molecule with a unique structure. It features a tetrahydro-furo[2',3':4,5]oxazolo[3,2-c]pyrimidine core, which is a fused ring system consisting of a furan and an oxazole connected through a pyrimidine ring. The compound has two hydroxyl groups, one at the 3c position and another as a hydroxymethyl group at the 2t position, indicating the presence of alcohol and ether functional groups. The stereochemistry is specified with the "3aS" and "3ar,9ac" notations, indicating the specific arrangement of atoms in three-dimensional space. The compound also has a 6,8-dione functional group, suggesting the presence of two carbonyl groups. This molecule is likely to be of interest in the field of medicinal chemistry or as a potential intermediate in the synthesis of biologically active compounds due to its intricate structure and functional groups.

17245-47-5

Post Buying Request

17245-47-5 Suppliers

Recommended suppliers

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

17245-47-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17245-47-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,4 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17245-47:
(7*1)+(6*7)+(5*2)+(4*4)+(3*5)+(2*4)+(1*7)=105
105 % 10 = 5
So 17245-47-5 is a valid CAS Registry Number.

17245-47-5Relevant academic research and scientific papers

Synthesis of 5-arylthiouridines via electrophilic substitution of 5- bromouridines with diaryl disulfides

Hirota, Kosaku,Tomishi, Tetsuo,Maki, Yoshifumi,Sajiki, Hironao

, p. 161 - 173 (2007/10/03)

Novel synthetic method of 5-arylthiouridine derivatives is described. Treatment of 5-bromo-2',3'-O-isopropylideneuridine (1a) with diaryl disulfides in the presence of sodium hydride at ambient temperature gave the 5-arylthiouridines (2) in moderate yields. The present method is devised by virtue of a combination of efficient participation of the 5'-hydroxy group onto the uracil ring and the electrophilic nature of diaryl disulfide, which was applied to the synthesis of 5-arylthio-1-β-D-arabinofuranosyluracils (8).

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 17245-47-5