Welcome to LookChem.com Sign In|Join Free

CAS

  • or

463297-75-8

Post Buying Request

463297-75-8 Suppliers

Recommended suppliersmore

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

463297-75-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 463297-75-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,3,2,9 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 463297-75:
(8*4)+(7*6)+(6*3)+(5*2)+(4*9)+(3*7)+(2*7)+(1*5)=178
178 % 10 = 8
So 463297-75-8 is a valid CAS Registry Number.

463297-75-8Relevant articles and documents

A divergent synthesis of minor groove binders with tail group variation

Breen, David,Kennedy, Alan R.,Suckling, Colin J.

experimental part, p. 178 - 186 (2009/04/07)

A new synthesis of polyamide minor groove binders in which diversity is introduced by the nucleophilic substitution of a 2-sulfido-1,3,2- diazaphospholidinyloxy substituent by volatile secondary amine nucleophiles is described. Such a method has potential

Antimicrobial lexitropsins containing amide, amidine, and alkene linking groups

Anthony, Nahoum G.,Breen, David,Clarke, Joanna,Donoghue, Gavin,Drummond, Allan J.,Ellis, Elizabeth M.,Gemmell, Curtis G.,Helesbeux, Jean-Jacques,Hunter, Iain S.,Khalaf, Abedawn I.,Mackay, Simon P.,Parkinson, John A.,Suckling, Colin J.,Waigh, Roger D.

, p. 6116 - 6125 (2008/09/16)

The synthesis and properties of 80 short minor groove binders related to distamycin and the thiazotropsins are described. The design of the compounds was principally predicated upon increased affinity arising from hydrophobic interactions between minor groove binders and DNA. The introduction of hydrophobic aromatic head groups, including quinolyl and benzoyl derivatives, and of alkenes as linkers led to several strongly active antibacterial compounds with MIC for Staphylococcus aureus, both methicillin-sensitive and -resistant strains, in the range of 0.1-5 μg mL-1, which is comparable to many established antibacterial agents. Antifungal activity was also found in the range of 20-50 μg mL-1 MIC against Aspergillus niger and Candida albicans, again comparable with established antifungal drugs. A quinoline derivative was found to protect mice against S. aureus infection for a period of up to six days after a single intraperitoneal dose of 40 mg kg-1.

Synthesis of (E)-5-(2-arylvinyl)-2-(hetero)arylpyridines, (E)-2-(2-arylvinyl)-5-methoxycarbonylpyridines and (E,E)-2,5-bis(2-arylvinyl)pyridines as polarity and pH probes

Van der Eycken, Erik,Jidong, Zhang,Kilonda, Amuri,Compernolle, Frans,Toppet, Suzanne,Hoornaert, Georges,Van der Auweraer, Mark,Jackers, Carine,Verbouwe, Wouter,De Schryver, Frans C.

, p. 928 - 937 (2007/10/03)

In this report we describe the synthesis photophysical properties (E)-5-(2-arylvinyl)-2-(hetero)-and of various arylpyridines 7a-f, (E)-2-(2-arylvinyl)-5-methoxycarbonylpyridines 14a,b and (E,E)-2,5-bis(2-arylvinyl)pyridines 13a,b. The fluorescence spectr

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 463297-75-8