63002-97-1 Usage
Derivative of benzoic acid
The compound is derived from benzoic acid, a simple aromatic carboxylic acid.
Contains a nitro group and an amino group
The compound has a nitro group (-NO2) and an amino group (-NH2) attached to a benzene ring, which can affect its chemical reactivity and properties.
Attached to a benzene ring
The nitro and amino groups are attached to a benzene ring, a six-membered aromatic ring structure.
E configuration
The compound has an E configuration, indicating the spatial arrangement of the atoms around the double bond in the compound.
Building block in the synthesis of other organic compounds
The compound can be used as a building block in the synthesis of other organic compounds, allowing for the creation of more complex molecules.
Reagent in chemical reactions
The compound can be used as a reagent in chemical reactions, facilitating the formation of new bonds and the transformation of other compounds.
Suitable for various applications in organic chemistry and pharmaceutical research
The compound's structure and properties make it suitable for a range of applications in the field of organic chemistry and pharmaceutical research, including the development of new drugs and the study of chemical reactions and mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 63002-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,0 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63002-97:
(7*6)+(6*3)+(5*0)+(4*0)+(3*2)+(2*9)+(1*7)=91
91 % 10 = 1
So 63002-97-1 is a valid CAS Registry Number.
63002-97-1Relevant academic research and scientific papers
Synthesis of 2-(o-Arylideneaminophenyl)-3-(5-alkyl-1,3,4-thiadiazol-2-yl)quinazolin-4-ones as Potential Anthelmintic Agents
Shukla, J. S.,Singh, Mithilesh,Rastogi, Renu
, p. 306 - 307 (2007/10/02)
A series of 2-(o-arylideneaminophenyl)-3-(5-alkyl-1,3,4-thiadiazol-2-yl)quinazolin-4-ones (13-41) have been synthesised and screened for their cestodicidal activity against Hymenolepis nana infection in rats.Compound 19 has been found to be the most active member of the series showing 77.2percent clearance of infection at a dose of 250 mg/kg given for 3 days.
