Welcome to LookChem.com Sign In|Join Free
  • or
3-deoxy-1,2-O-(1-methylethylidene)-3-<(phenylmethoxy)methyl>-5-O-(phenylmethyl)-α-D-ribofuranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69827-91-4

Post Buying Request

69827-91-4 Suppliers

Recommended suppliers

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

69827-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69827-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,2 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69827-91:
(7*6)+(6*9)+(5*8)+(4*2)+(3*7)+(2*9)+(1*1)=184
184 % 10 = 4
So 69827-91-4 is a valid CAS Registry Number.

69827-91-4Relevant academic research and scientific papers

Stereoselective cyclopropanation in the synthesis of 3'-deoxy-3'-C-hydroxymethyl-2',3'-methylene-uridine

Komsta, Zofia,Mayes, Benjamin A.,Moussa, Adel,Shelbourne, Montserrat,Stewart, Alistair,Tyrrell, Andrew J.,Wallis, Laura L.,Weymouth-Wilson, Alexander C.,Yurek-George, Alexander

supporting information, p. 4878 - 4880 (2015/04/27)

The synthesis of the novel 2',3'-cyclopropane nucleoside 3'-deoxy-3'-C-hydroxymethyl-2',3'-methylene-uridine is described. Stereoselective construction of the cyclopropane ring was achieved via Simmons-Smith cyclopropanation of a benzyl protected silyl enol ether, which was itself derived from 1,2-O-isopropylidene-α-D-xylofuranose.

Syntheses and Biological Evaluations of 3'-Deoxy-3'-C-Branched-Chain-Substituted Nucleosides

Lin, Tai-Shun,Zhu, Ju-Liang,Dutschman, Ginger E.,Cheng, Yung-Chi,Prusoff, William H.

, p. 353 - 362 (2007/10/02)

Various 3'-deoxy-3'-C-(hydroxymethyl)-, 3'-deoxy-3'-C-(fluoromethyl)-, 3'-deoxy-3'-C-(azidomethyl)-, and 3'-deoxy-3'-C-(aminomethyl)-substituted nucleosides (total 12 compounds) have been synthesized and evaluated against L1210, P388, S-180, and CCRF-CEM

Synthesis and antiviral activity of novel isonucleoside analogs

Tino,Clark,Field,Jacobs,Lis,Michalik,McGeever-Rubin,Slusarchyk,Spergel,Sundeen,Tuomari,Weaver,Young,Zahler

, p. 1221 - 1229 (2007/10/02)

A series of branched-chain sugar isonucleosides was synthesized and evaluated for antiviral activity against herpesviruses. The preparation of homochiral [3S-(3α,4β,5α)]-2-amino-1,9-dihydro-9-[tetrahydro-4,5- bis(hydroxymethyl)-3-furanyl]-6H-purin-6-one (

Purinyl tetrahydrofurans

-

, (2008/06/13)

Antiviral activity is exhibited by compounds having the formula STR1 and pharmaceutically acceptable salts thereof wherein R1 is a purine or pyrimidine base or an analog thereof and R2 and R3 are independently hydrogen, --

SYNTHESIS OF OXETANOCIN

Wilson, F. X.,Fleet, G. W. J.,Vogt, K.,Wang, Y.,Witty, D. R.,et al.

, p. 6931 - 6934 (2007/10/02)

A low yield synthesis of oxetanocin and its α-epimer by reaction of adenine with a protected 3-hydroxymethyl-2-chlorooxetane is described; attempts to synthesise other C-2'alkyl analogues of oxetanocin by analogous reactions indicate a limitation of this strategy for the synthesis of oxetane nucleosides.An intermediate for the synthesis of C-nucleoside analogues of oxetanocin is reported.

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 69827-91-4