Welcome to LookChem.com Sign In|Join Free
  • or
N-(9-((2R,3R,4S,5R)-3-azido-4-(tert-butyldimethylsilyloxy)-5(hydroxymethyl) tetrahydro-furan-2-yl)-9H-purin-6-yl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1242450-41-4

Post Buying Request

1242450-41-4 Suppliers

Recommended suppliers

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

1242450-41-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1242450-41-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,2,4,5 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1242450-41:
(9*1)+(8*2)+(7*4)+(6*2)+(5*4)+(4*5)+(3*0)+(2*4)+(1*1)=114
114 % 10 = 4
So 1242450-41-4 is a valid CAS Registry Number.

1242450-41-4Relevant academic research and scientific papers

Decoding the logic of the tRNA regiospecificity of nonribosomal femX Wv aminoacyl transferase www.angewandte.org

Fonvielle, Matthieu,Chemama, Maryline,Lecerf, Maxime,Villet, Regis,Busca, Patricia,Bouhss, Ahmed,Etheve-Quelquejeu, Melanie,Arthur, Michel

supporting information; experimental part, p. 5115 - 5119 (2010/11/04)

Natural selection: Replacement of the 3′-OH group of Ala-tRNA Ala with 3′-H affected FemXWv-catalyzed aminoacyl transfer from the 2 -position, but not substrate binding. The ability of FemXWv to bind and transacylate the 3′-O-Ala isomer initially formed by alanyl-tRNA synthetase (AlaRS) may be crucial for efficient competition with the ribosome (see scheme). (Figure Presented).

The synthesis of diverse adenosine 5'-phosphonate analogues as chain terminators against hepatitis C virus (HCV)

Kim, Bo-Seung,Kim, Beom-Tae,Hwang, Ki-Jun

experimental part, p. 1643 - 1648 (2010/10/19)

Adenosine 5'-phosphonates have been reported as potential chain terminators against Hepatitis C virus (HCV); therefore, we developed convenient sequences for synthesis of modified adenosine 5'-phosphonates in which the hydroxyl group at 2' or 3'-position of the sugar moiety is substituted with the azido or amino group and the oxymethyl group at the 4'-position is modified by the ethylene or vinyl group. This synthetic sequence can provide six adenosine 5'-phosphonates via one protocol, and is considered to be very efficient and a convenient route of synthesis. An assay of adenosine 5'-phosphonate analogues (1, 2, 3, 4, 5, and 6) against HCV infection is now in progress.

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 1242450-41-4