93415-46-4 Usage
Molecular Structure
1H-Pyrazole, 4,5-dihydro-1-acetyl-3-(2-(3-chloro-2-(1H-indol-3-yl)-4-oxo-1-azetidinyl)phenyl)-5-(3-chlorophenyl)is a complex organic compound with a pyrazole ring and multiple functional groups attached to it.
Functional Groups
The compound contains an acetyl group (CH3CO-), a 3-chlorophenyl group (C6H4Cl), a 3-chloro-2-(1H-indol-3-yl)-4-oxo-1-azetidinyl group, and a phenyl group (C6H5-) attached to the pyrazole ring.
Pyrazole Ring
The compound has a five-membered nitrogen-containing heterocycle, which is the main structural feature of 1H-Pyrazole, 4,5-dihydro-1-acetyl-3-(2-(3-chloro-2-(1H-indol-3-yl)-4-oxo-1-azetidinyl)phenyl)-5-(3-chlorophenyl)-.
Potential Pharmacological Activity
The complex structure of the compound suggests that it may have potential pharmacological activity, possibly in the areas of medicinal chemistry and drug development.
Further Investigation
The specific properties and potential applications of 1H-Pyrazole, 4,5-dihydro-1-acetyl-3-(2-(3-chloro-2-(1H-indol-3-yl)-4-oxo-1-azetidinyl)phenyl)-5-(3-chlorophenyl)- would require further investigation and analysis to determine its potential uses and effectiveness.
Check Digit Verification of cas no
The CAS Registry Mumber 93415-46-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,1 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93415-46:
(7*9)+(6*3)+(5*4)+(4*1)+(3*5)+(2*4)+(1*6)=134
134 % 10 = 4
So 93415-46-4 is a valid CAS Registry Number.
93415-46-4Relevant academic research and scientific papers
Synthesis of 1-Acetyl-5-aryl-3--2-pyrazolines
Kumar, Ashok,Sinha, Jagdish N.,Bhargava, Krishna P.,Shanker, Kirpa
, p. 589 - 591 (2007/10/02)
Substituted-2'-(indol-3-yl-methyleneamino)chalkones (IIa), synthesized by the condensation of 2-(indol-3-yl-methyleneamino)acetophenone (Ia) with different aromatic aldehydes, undergo cyclisation with hydrazine hydrate in the presence of gl. acetic acid t