74169-54-3 Usage
Uses
Used in Pharmaceutical Industry:
1-(4-chlorophenyl)-3,4-dimethyl-Pyrano[2,3-c]pyrazol-6(1H)-one is used as a potential candidate for drug development due to its pharmacological and biological activities. Its unique structure may allow it to interact with specific biological targets, making it a promising compound for the creation of new medications.
Used in Material Science:
In the field of material science, 1-(4-chlorophenyl)-3,4-dimethyl-Pyrano[2,3-c]pyrazol-6(1H)-one may find applications due to its specific chemical and physical properties. Its heterocyclic structure could be utilized in the development of new materials with tailored properties for various applications.
Used in Organic Synthesis:
1-(4-chlorophenyl)-3,4-dimethyl-Pyrano[2,3-c]pyrazol-6(1H)-one can be used as a synthetic building block or intermediate in the synthesis of more complex organic compounds. Its unique structure may facilitate the creation of novel molecules with specific functions or properties.
Further research and study of 1-(4-chlorophenyl)-3,4-dimethyl-Pyrano[2,3-c]pyrazol-6(1H)-one's properties and potential applications are necessary to fully understand its capabilities and maximize its utility in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 74169-54-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,6 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74169-54:
(7*7)+(6*4)+(5*1)+(4*6)+(3*9)+(2*5)+(1*4)=143
143 % 10 = 3
So 74169-54-3 is a valid CAS Registry Number.
74169-54-3Relevant academic research and scientific papers
Synthesis and chemistry of N-arylated pyrano[2,3-c]pyrazoles
Samaritoni, J. Geno,Thornburgh, Scott,Graupner, Paul R.,Cooper, David H.
, p. 1389 - 1393 (2008/09/18)
(Chemical Equation Presented) Novel N2-arylated pyrano[2,3-c]pyrazol-6-ones 2 can be prepared in a selective manner by generating the anion of 1 (R=H) with lithium hexamethyldisilazide in DMF and quenching with activated aryl halides. Sterically demanding
ETUDE DE LA REACTIVITE DU 3-AMINO-2-BUTENOATE D'ETHYLE VIS-A-VIS D'AZOLINE-5-ONES.
Maquestiau, A.,Eynde, J.-J. Vanden,Manderlier, R.
, p. 1073 - 1082 (2007/10/02)
Various 1,3-disubstituted pyrazolin-5-ones, 3-phenylisoxazolin-5-one and 2-phenyloxazolin-5-one react with ethyl 3-amino-2-butenoate to yield compounds resulting from the elimination of ammonia between the precursors; subsequent intramolecular cyclization
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.
