132631-84-6 Usage
Chemical structure
1-Phenyl-3-pentafluoroethyl-4-hydro-5-hydroxypyrazole is a pyrazole derivative with a unique structure containing phenyl, pentafluoroethyl, and hydroxy groups.
Stability
The pentafluoroethyl group provides the compound with significant chemical stability and resistance to degradation.
Unique functional group combination
The presence of both hydroxyl and pentafluoroethyl groups makes this compound relatively uncommon in chemical compounds, offering interesting opportunities for the development of novel drugs and pesticides.
Potential applications
1-Phenyl-3-pentafluoroethyl-4-hydro-5-hydroxypyrazole has potential applications in the pharmaceutical and agrochemical industries due to its unique structure and properties.
Need for further research
Further studies on the properties and potential uses of this compound are needed to fully understand its applications and potential benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 132631-84-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,6,3 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132631-84:
(8*1)+(7*3)+(6*2)+(5*6)+(4*3)+(3*1)+(2*8)+(1*4)=106
106 % 10 = 6
So 132631-84-6 is a valid CAS Registry Number.
132631-84-6Relevant articles and documents
New one-pot synthesis of 4-hydroxyimino-5-polyfluoroalkylpyrazol-3-ones, their structure and biological activity
Burgart, Yanina V.,Agafonova, Natalya A.,Shchegolkov, Evgeny V.,Maslova, Vera V.,Triandafilova, Galina A.,Solodnikov, Sergey Yu.,Krasnykh, Olga P.,Saloutin, Victor I.
, p. 52 - 59 (2019/02/25)
[Figure not available: see fulltext.] We propose different methods for the synthesis of 4-hydroxyimino-5-polyfluoroalkylpyrazol-3-ones. The simplest and most convenient procedure relies on sequential one-pot treatment of polyfluoroalkyl-3-oxoesters with hydrazine and sodium nitrite in acetic acid. It was established that 4-hydroxyimino-5-polyfluoroalkylpyrazol-3-ones exist in solid state and in solutions as mixtures of Z,Е-isomers of the hydroxyimine tautomer. The synthesized compounds were characterized with respect to in vivo analgesic activity and acute toxicity.
5-FLUORO-SUBSTITUTED PYRAZOLES
Bargamova, M. D.,Motsishkite, S. M.,Knunyants, I. L.
, p. 2338 - 2344 (2007/10/02)
A preparative method was developed for the synthesis of 5-fluoro-substituted pyrazoles by the reaction of fluoroolefins with substituted hydrazines in the presence of triethylamine.The fluorine atom at the C5 position of the pyrazoles obtained
