127142-19-2 Usage
Molecular structure
A complex organic compound consisting of a carbothioamide group, a hydrazinecarbothioamide group, and a tricyclo[3.3.1.1^3,7^]dec-1-yl group connected to a pyridin-2-yl group through an ethylidene linkage.
Functional groups
Carbothioamide, hydrazinecarbothioamide, and tricyclo[3.3.1.1^3,7^]dec-1-yl groups, as well as a pyridin-2-yl group connected via an ethylidene linkage.
Potential biological activity
The complex structure of the compound suggests that it may have potential biological activity, making it a candidate for further investigation in pharmaceutical or agrochemical applications.
Complexity
Due to the intricate nature of the compound, it may exhibit a range of properties and reactivities that require careful study and analysis.
Handling precautions
Because of the potential reactivity and unknown properties, 2-({(2E)-2-[1-(pyridin-2-yl)ethylidene]hydrazinyl}carbothioyl)-N-(tricyclo[3.3.1.1~3,7~]dec-1-yl)hydrazinecarbothioamide should be handled with care and in accordance with proper safety protocols.
Investigation requirements
Thorough investigation of the compound's properties and functions is necessary to fully understand its potential applications and limitations.
Check Digit Verification of cas no
The CAS Registry Mumber 127142-19-2 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, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 127142-19:
(8*1)+(7*2)+(6*7)+(5*1)+(4*4)+(3*2)+(2*1)+(1*9)=102
102 % 10 = 2
So 127142-19-2 is a valid CAS Registry Number.
127142-19-2Relevant academic research and scientific papers
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
