Welcome to LookChem.com Sign In|Join Free

CAS

  • or

79083-29-7

Post Buying Request

79083-29-7 Suppliers

Recommended suppliersmore

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

79083-29-7 Usage

General Description

The chemical "(2R,3R,4R,5S)-3,4-bis(benzyloxy)-2-((benzyloxy)methyl)-5-methoxytetrahydrofuran" is a complex compound with multiple benzyl and methoxy groups attached to a tetrahydrofuran ring. The compound has a stereochemistry with a 2R, 3R, 4R, 5S configuration, indicating the specific arrangement of substituents around the tetrahydrofuran ring. The presence of benzyl and methoxy groups suggests that this compound may have potential applications in organic synthesis, medicinal chemistry, or as a building block for the synthesis of more complex molecules. The detailed structure and stereochemistry of the compound make it an interesting target for further research and potential use in diverse chemical and pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 79083-29-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,8 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79083-29:
(7*7)+(6*9)+(5*0)+(4*8)+(3*3)+(2*2)+(1*9)=157
157 % 10 = 7
So 79083-29-7 is a valid CAS Registry Number.

79083-29-7Downstream Products

79083-29-7Relevant articles and documents

HCV POLYMERASE INHIBITORS

-

, (2013/06/27)

The invention provides compounds of the formula:(I) which are of use in the treatment or prophylaxis of hepatitis C virus infection, and related aspects.

Anodic coupling reactions and the synthesis of C-glycosides

Xu, Guoxi,Moeller, Kevin D.

supporting information; experimental part, p. 2590 - 2593 (2010/08/22)

A convenient, two-step procedure has been developed for converting sugar derivatives into C-glycosides containing a masked aldehyde functional group. The chemistry takes advantage of an anodic coupling reaction between an electron-rich olefin and an alcohol. The sequence works for the formation of both furanose and pyranose derivatives if less polarized vinyl sulfide derived radical cation intermediates are used. With more polarized enol ether derived radical cations, the cyclizations work best for the formation of furanose derivatives where the rate of five-membered ring formation precludes elimination reactions triggered by the radical cation.

Synthesis of β-D-ribofuranosyl-(1→3)-α-L-rhamnopyranose by in situ activating glycosylation using 1-OH sugar derivative and Me3SiBr-CoBr2-Bu4NBr-molecular sieves 4A system

Hirooka,Mori,Sasaki,Koto,Shinoda,Morinaga

, p. 1679 - 1694 (2007/10/03)

Β-D-Ribofuranosyl-(1→3)-α-L-rhamnopyranosyl-(1→3)- L-rhamnopyranose, the trisaccharide repeating unit of the C. freundii O28, 1c O-specific polysaccharide, was synthesized using in situ activating glycosylation of the 1-OH sugar derivatives and a reagent mixture of trimethylsilyl bromide, cobalt(II) bromide, tetrabutylammonium bromide, and molecular sieves 4A. Regioselective tritylation was useful for synthesizing the 3-OH derivatives of methyl, allyl, and benzyl α-L-rhamnosides.

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

What can I do for you?
Get Best Price

Get Best Price for 79083-29-7