127142-05-6 Usage
Chemical class
Hydrazine-based compound
Explanation
The compound is based on a hydrazine structure, which consists of nitrogen and hydrogen atoms.
Explanation
The compound's composition includes these five elements in its molecular structure.
Explanation
The compound's molecular formula represents the number of each element's atoms in the molecule.
Explanation
The molecular weight is the mass of one mole of the compound, calculated from the atomic weights of the elements present.
Explanation
The compound is mainly used for research purposes and the development of new pharmaceuticals.
Explanation
The compound's structure consists of these three key elements, which contribute to its potential properties and applications.
Explanation
The compound may be a promising candidate for the development of new drugs, and further studies could reveal its biological and pharmacological properties.
Elements present
Carbon (C), Hydrogen (H), Nitrogen (N), Sulfur (S), and Fluorine (F)
Molecular weight
445.48 g/mol
Primary use
Chemical research and pharmaceutical development
Structural features
Pyridine ring, ethylidene hydrazine group, and trifluoromethyl phenyl group
Potential target
Drug design and synthesis
Check Digit Verification of cas no
The CAS Registry Mumber 127142-05-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,1,4 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 127142-05:
(8*1)+(7*2)+(6*7)+(5*1)+(4*4)+(3*2)+(2*0)+(1*5)=96
96 % 10 = 6
So 127142-05-6 is a valid CAS Registry Number.
127142-05-6Relevant articles and documents
2-Acetylpyridine thiocarbonohydrazones. Potent inactivators of herpes simplex virus ribonucleotide reductase
Blumenkopf,Harrington,Koble,Bankston,Morrison Jr.,Bigham,Styles,Spector
, p. 2306 - 2314 (2007/10/02)
A series of 2-acetylpyridine thiocarbonohydrazones was synthesized for evaluation as potential antiherpetic agents. The compounds were prepared by the condensation of 2-acetylpyridine with thiocarbonohydrazide followed by treatment with isocyanates or iso