74618-03-4 Usage
Uses
Used in Pharmaceutical Industry:
2,4-Dihydrochromeno[4,3-c]pyrazole is used as a pharmaceutical candidate for its potential therapeutic applications. Its anti-inflammatory, analgesic, and antitumor properties make it a promising compound for the development of new drugs to treat various diseases and conditions.
Used in Medicinal Chemistry Research:
2,4-Dihydrochromeno[4,3-c]pyrazole is used as a subject of study in medicinal chemistry research. Its unique molecular structure and properties allow researchers to explore its potential in the development of novel therapeutic agents and to understand its mechanism of action in treating various diseases.
Used in Drug Development:
2,4-Dihydrochromeno[4,3-c]pyrazole is used in the process of drug development to create new pharmaceuticals with improved efficacy and safety profiles. Its diverse pharmacological activities and potential for further modification make it a valuable compound for the design and synthesis of innovative drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 74618-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,1 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 74618-03:
(7*7)+(6*4)+(5*6)+(4*1)+(3*8)+(2*0)+(1*3)=134
134 % 10 = 4
So 74618-03-4 is a valid CAS Registry Number.
74618-03-4Relevant academic research and scientific papers
“On water” cascade synthesis of benzopyranopyrazoles and their macrocycles
Muthusamy, Sengodagounder,Gangadurai, Chinnakuzhanthai
supporting information, p. 1501 - 1505 (2018/03/21)
Reported herein is an intramolecular 1,3-dipolar cycloaddition strategy for rapid entry into benzopyranopyrazoles (BPP) on water medium as “open flask chemistry” approach. The in situ generation of diazo functionality in two-step sequence from the appropr
Intramolecular Cycloaddition Reactions of N-Sulfonyl Nitrile Imides Bearing Alkenyl Groups
Shimizu, Tomio,Hayashi, Yoshiyuki,Nagano, Yoshio,Teramura, Kazuhiro
, p. 429 - 434 (2007/10/02)
The reaction of the p-tolyl(or phenyl)sulfonylhydrazones of some 2-(alkenyloxy)benzaldehydes with lead tetraacetate leads, via the nitrile imide intermediates, Ar-C(+)=N-N(-)-SO2-C6H4-X-p, to intramolecular 1,3-dipolar cycloadducts and 1-acetyl-2-aroyl-1-
