80542-50-3 Usage
General Description
2-[(2,6-Dichloropyridin-4-yl)thio]acetic acid is a chemical compound that falls under the category of organohalogen compounds, more specifically, a heteroaryl halide. The prefix "di" indicates the presence of two chlorine atoms, while "pyridin" refers to a basic heterocyclic organic compound. Furthermore, the term "thio" in its name relates to its containing sulphur, and "acetic acid" suggests a carboxylic acid group in the structure. The molecular structure of this compound comprises several types of functional groups that give it a diverse range of potential properties and uses, possibly including roles in the development of pharmaceuticals, agrochemicals, and materials science. However, its specific characteristics, uses, and impact on human health or the environment would need further studying or extrapolating from available data on related chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 80542-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,4 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80542-50:
(7*8)+(6*0)+(5*5)+(4*4)+(3*2)+(2*5)+(1*0)=113
113 % 10 = 3
So 80542-50-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H5Cl2NO2S/c8-5-1-4(2-6(9)10-5)13-3-7(11)12/h1-2H,3H2,(H,11,12)
80542-50-3Relevant articles and documents
Synthesis and anti-MRSA activity of novel cephalosporin derivatives
D'Andrea, Stan V.,Bonner, Daniel,Bronson, Joanne J.,Clark, Junius,Denbleyker, Ken,Fung-Tomc, Joan,Hoeft, Shelley E.,Hudyma, Thomas W.,Matiskella, John D.,Miller, Raymond F.,Misco, Peter F.,Pucci, Michael,Sterzycki, Roman,Tsai, Yuan,Ueda, Yasutsuga,Wichtowski, John A.,Singh, Janak,Kissick, Thomas P.,North, Jeffery T.,Pullockaran, Annie,Humora, Michael,Boyhan, Brenda,Vu, Truc,Fritz, Alan,Heikes,Fox, Rita,Godfrey, Jollie D.,Perrone, Robert,Kaplan, Murray,Kronenthal, David,Mueller, Richard H.
, p. 5687 - 5698 (2000)
Cephalosporin derivatives containing a unique combination of lipophilic C-7 sidechains and polar C-3 thiopyridinium groups were synthesized and found to exhibit potent anti-MRSA activity in vitro and in vivo. The optimum C-7 sidechains utilized were 2,5-dichlorophenylthioacetamido and 2,6-dichloropyrid-4-ylthioacetamido. The C-3 thiopyridinium rings were substituted at nitrogen with amino acid and pyruvic acid groups that were designed to confer aqueous solubility as required for IV formulation. This paper describes the characteristics of these novel cephalosporins and highlights synthetic methods developed to allow their practical, large-scale syntheses. (C) 2000 Elsevier Science Ltd.
