947-82-0 Usage
General Description
2,4-Dihydro-4,4,5-trimethyl-2-phenyl-3H-pyrazol-3-one is a chemical compound that belongs to the class of pyrazolones. It is a yellow crystalline powder with a molecular formula of C13H16N2O and a molecular weight of 216.28 g/mol. 2,4-Dihydro-4,4,5-trimethyl-2-phenyl-3H-pyrazol-3-one is used in the synthesis of pharmaceuticals and has been studied for its potential antioxidant and anti-inflammatory properties. It is also utilized as a light stabilizer in various industrial applications. However, its precise uses and applications are still being explored, and further research is needed to fully understand its potential benefits and risks.
Check Digit Verification of cas no
The CAS Registry Mumber 947-82-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 947-82:
(5*9)+(4*4)+(3*7)+(2*8)+(1*2)=100
100 % 10 = 0
So 947-82-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H14N2O/c1-9-12(2,3)11(15)14(13-9)10-7-5-4-6-8-10/h4-8H,1-3H3
947-82-0Relevant articles and documents
Palladium-catalyzed double C-H activation: One-pot synthesis of benzo[c]pyrazolo[1,2-a]cinnolin-1-ones from 5-pyrazolones and aryl iodides
Fan, Zhoulong,Wu, Kui,Xing, Li,Yao, Qizheng,Zhang, Ao
, p. 1682 - 1684 (2014)
A palladium-catalyzed dual C-H activation to construct C-C/C-N bonds for one-pot synthesis of benzo[c]pyrazolo[1,2-a]cinnolin-1-ones is successfully developed. This approach involves using a pyrazolone moiety as an internal directing group for C-H activation, and provides a flexible strategy to access this polycyclic skeleton.
Synthesis and structure-activity relationships of miticidal 4,5- dihydropyrazole-5-thiones
Tada,Motoki,Takahashi,Miyata,Takechi,Uchida,Takagi
, p. 165 - 173 (2007/10/03)
A series of novel 4,5-dihydropyrazole-5-thiones (DHPs) was synthesised by treating the corresponding dihydropyrazolones with Lawesson's reagent and evaluated for miticidal activity against two-spotted spider mites (Tetranychus urticae Koch). Of these, 3-(