60403-69-2 Usage
Chemical structure
A derivative of phenyl and furan with a 3,5-dichloro-2-hydroxyphenyl group and a 2-furyl group attached to a prop-2-en-1-one core.
Appearance
Yellow to brown crystalline solid.
Solubility
Insoluble in water.
Reactivity
Acts as an α,β-unsaturated ketone, making it useful in the synthesis of other organic compounds.
Applications
a. Used in the production of pharmaceuticals and agrochemicals.
b. Studied for potential anti-inflammatory properties.
c. Studied for potential antioxidant properties.
Interest
Compound of interest in the development of new drugs and therapies due to its potential anti-inflammatory and antioxidant properties.
Check Digit Verification of cas no
The CAS Registry Mumber 60403-69-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,0 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60403-69:
(7*6)+(6*0)+(5*4)+(4*0)+(3*3)+(2*6)+(1*9)=92
92 % 10 = 2
So 60403-69-2 is a valid CAS Registry Number.
60403-69-2Relevant academic research and scientific papers
Synthesis of pyrazolines, isoxazoles and cyanopyridines as potential antimicrobial agents
Shah, Manish,Patel, Pankaj,Korgaokar, Sushil,Parekh, Hansa
, p. 1282 - 1286 (2007/10/03)
3,5-Dichloro-2-hydroxyacetophenone 1 on treatment with aromatic aldehydes yields 3,5-dichloro-2-hydroxy-ω-arylidine acetophenones 2a-j which on cyclisation with hydrazine hydrate, hydroxylamine hydrochloride and malononitrile furnishes the corresponding 3
