85094-16-2 Usage
Chemical Structure
1-(2-Chloro-phenyl)-3,4-dimethyl-1H-pyrano[2,3-c]pyrazol-6-one is a complex chemical compound with a pyrano[2,3-c]pyrazol-6-one core and 1-(2-Chloro-phenyl) and 3,4-dimethyl substituents.
Pharmaceutical Applications
1-(2-Chloro-phenyl)-3,4-dimethyl-1H-pyrano[2,3-c]pyrazol-6-one is used in various pharmaceutical applications, including as a building block for the synthesis of other compounds.
Research Applications
It is also used in research applications, particularly in the field of medicinal chemistry.
Potential Therapeutic Agent
1-(2-Chloro-phenyl)-3,4-dimethyl-1H-pyrano[2,3-c]pyrazol-6-one has been studied for its potential as a therapeutic agent.
Anti-Inflammatory Properties
The compound has been investigated for its potential anti-inflammatory properties.
Antibacterial Properties
It has also been studied for its potential antibacterial properties.
Antiviral Properties
The compound has been researched for its potential antiviral properties.
Anticancer Properties
1-(2-Chloro-phenyl)-3,4-dimethyl-1H-pyrano[2,3-c]pyrazol-6-one has been studied for its potential anticancer properties.
Further Research and Development
Due to its potential therapeutic properties, 1-(2-Chloro-phenyl)-3,4-dimethyl-1H-pyrano[2,3-c]pyrazol-6-one is a valuable compound for further research and development in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 85094-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,9 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85094-16:
(7*8)+(6*5)+(5*0)+(4*9)+(3*4)+(2*1)+(1*6)=142
142 % 10 = 2
So 85094-16-2 is a valid CAS Registry Number.
85094-16-2Relevant academic research and scientific papers
Pyranopyrazoles. II (1). Synthesis and Reactions of 1H,6H-Pyranopyrazol-6-ones
Khan, Misbahul Ain,Cosenza, Alina Guerra,Ellis, Gwynn Pennant
, p. 1077 - 1085 (2007/10/02)
Various 1H,6H-pyranopyrazol-6-ones (III-XXIII) were obtained from β-keto esters and 1H-pyrazol-5-ones or hydrazines.Nitrations, chlorinations and brominations of these pyranopyrazoles were also carried out giving the corresponding derivatives (XXIV-LXIV).The pyrone ring is the more reactive one by the addition-elimination route.
