83749-78-4 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The compound is composed of a fused ring system containing both carbon and nitrogen atoms.
Explanation
The presence of a chlorine atom in the compound contributes to its unique properties and potential applications.
Explanation
The phenyl group is an aromatic ring that is connected to the core structure, further modifying the compound's properties.
Explanation
The compound is primarily synthesized in laboratories and is not typically found in natural environments.
Explanation
Due to its unique structure, the compound is valuable for scientific investigations and understanding its potential applications.
Explanation
The compound's structure and properties make it a candidate for the development of new drugs and therapeutic agents.
Explanation
The full potential of 1-Chloro-4-phenyl-5H-pyridazino[4,5-b]indole is not yet fully understood, and ongoing research aims to uncover its capabilities in different areas.
Chemical Structure
Heterocyclic compound with a pyridazinoindole core
Chlorine Atom
Attached to the molecule
Phenyl Group
Attached to the pyridazinoindole core
Natural Occurrence
Not commonly found in nature
Usage
Mainly used in research and experimental studies
Potential Applications
Medicinal chemistry and pharmaceutical research
Ongoing Research
Uses and applications in various fields are still being explored
Check Digit Verification of cas no
The CAS Registry Mumber 83749-78-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,4 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 83749-78:
(7*8)+(6*3)+(5*7)+(4*4)+(3*9)+(2*7)+(1*8)=174
174 % 10 = 4
So 83749-78-4 is a valid CAS Registry Number.
83749-78-4Relevant academic research and scientific papers
SYNTHESIS OF 5H-PYRIDAZOINDOLES BY CONDENSATION OF 2-ACYLINDOLE-3-CARBOXYLIC ACIDS WITH HYDRAZINE
Zhungietu, G. I.,Zorin, L. M.,Gorgos, V. I.,Rekhter, M. A.
, p. 811 - 813 (2007/10/02)
5H-Pyridazoindol-1-ones were obtained by heating 2-acetylindole-3- or 2-aroylindole-3-carboxylic acids with hydrazine hydrate in ethylene glycol or alcohol. 1-Chloro-5H-pyridazoindoles are formed by treatment of 5H-pyridazoindol-1-one
