67056-25-1 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-hydroxyethyl)-3,4-dimethylpyrano[2,3-c]pyrazol-6(1H)-one is used as a potential drug candidate for its possible anti-inflammatory, anti-cancer, or antiviral properties. 1-(2-hydroxyethyl)-3,4-dimethylpyrano[2,3-c]pyrazol-6(1H)-one's unique structure and the presence of a hydroxyethyl group and dimethyl substituents make it a promising candidate for the development of new medications to treat various diseases and conditions.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 1-(2-hydroxyethyl)-3,4-dimethylpyrano[2,3-c]pyrazol-6(1H)-one is used as a subject of study for its potential pharmacological activities. Researchers are interested in exploring the compound's biological activities and its potential applications in the development of new drugs and therapies.
Used in Drug Design and Development:
1-(2-hydroxyethyl)-3,4-dimethylpyrano[2,3-c]pyrazol-6(1H)-one is used as a starting point for drug design and development. Its unique structure and potential pharmacological properties make it an attractive molecule for the creation of new drugs with improved efficacy and reduced side effects.
Used in Chemical Synthesis:
1-(2-hydroxyethyl)-3,4-dimethylpyrano[2,3-c]pyrazol-6(1H)-one can also be used in chemical synthesis as a building block or intermediate for the development of other complex molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 67056-25-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,5 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 67056-25:
(7*6)+(6*7)+(5*0)+(4*5)+(3*6)+(2*2)+(1*5)=131
131 % 10 = 1
So 67056-25-1 is a valid CAS Registry Number.
67056-25-1Relevant academic research and scientific papers
Condensation of N-3-substituted 5-pyrazolones with esters of β-keto acids. Synthesis of pyrano[2,3-c]pyrazol-6-ones
Nam,Grandberg
, p. 326 - 330 (2008/02/03)
N-Substituted 5-pryazolones undergo thermal condensation with esters of β-keto acids, losing water and alcohol molecules, to form N-substituted pyrano[2,3-c]pyrazol-6-ones. The pyran ring in these products is readily cleaved by the action of alkali to give the corresponding salts of unsaturated acids. 2006 Springer Science+Business Media, Inc.
Studies on heterocyclic compounds. 6. Synthesis and analgesic and antiinflammatory activities of 3,4-dimethylpyrano[2,3-c]pyrazol-6-one derivatives
Kuo,Huang,Nakamura
, p. 539 - 544 (2007/10/02)
A series of new 1- and 2-substituted 3,4-dimethylpyrano[2,3-c]pyrazol-6-one derivatives and 1-substituted 1,6 dihydro-4-methyl-6-oxopyrano[2,3-c]pyrazole-3-acetic acids were synthesized and examined for their analgesic and antiinflammatory activities. Mos
