64222-39-5 Usage
Chemical Family
Pyrrole
A heterocyclic aromatic organic compound consisting of a five-membered ring with four carbon atoms and one nitrogen atom.
Molecular Structure
2-(4-chlorophenyl)-1-ethenyl-
A pyrrole ring substituted with a 4-chlorophenyl group and an ethenyl group.
Pharmaceutical industry
May be used as an active ingredient or intermediate in the synthesis of drugs.
Agrochemicals
Could be used as a building block in the development of pesticides or herbicides.
Materials science
May contribute to the development of new materials with unique properties.
Unique chemical properties
The presence of the 4-chlorophenyl and ethenyl groups may impart unique reactivity and properties to the compound.
Biological activity
The compound may possess biological activity, making it a potential candidate for further research and development.
Handle with care
As with all chemicals, 1H-Pyrrole, 2-(4-chlorophenyl)-1-ethenylshould be handled with care and according to proper safety protocols.
Minimize potential risks
Follow safety guidelines to reduce the risk of accidents or exposure to harmful effects.
Check Digit Verification of cas no
The CAS Registry Mumber 64222-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,2 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64222-39:
(7*6)+(6*4)+(5*2)+(4*2)+(3*2)+(2*3)+(1*9)=105
105 % 10 = 5
So 64222-39-5 is a valid CAS Registry Number.
64222-39-5Relevant academic research and scientific papers
NUCLEOPHILIC ADDITION TO ALKYNES IN SUPERBASIC CATALYTIC SYSTEMS. V. VINYLATION OF KETOXIMES
Tarasova, O. A.,Korostova, S. E.,Mikhaleva, A. I.,Sobenina, L. N.,Nesterenko, R. N.,et al.
, p. 863 - 869 (2007/10/02)
The nucleophilic addition of the oximes of aliphatic, aromatic, and heteroaromatic ketones to acetylene in the superbasic heterophase potassium hydroxide-DMSO system was studied.The vinylation of ketoximes not containing a CH2 group at the α position to the oxime function goes well, and the yields of the O-vinyloximes are 38-72percent.With such a group and with electronegative substituents in the aromatic ring of the ketoxime rapid heterocyclization of the O-vinyloximes occurs under the reaction conditions, giving the corresponding 2-substituted pyrroles.
PYRROLES FROM KETOXIMES AND ACETYLENE. 1,2-DICHLOROETHANE IN PLACE OF ACETYLENE IN THE SYNTHESIS OF 2-ARYLPYRROLES
Korostova, S. E.,Mikhaleva, A. I.,Sobenina, L. N.,Shevchenko, S. G.,Polovnikova, R. I.
, p. 436 - 438 (2007/10/02)
In reaction with 1,2-dichloroethane in the potassium hydroxide-DMSO system 100-125 deg C methyl allyl ketone oximes form 2-arylpyrroles with yields of up to 69percent.The yield of the simultaneously formed N-vinyl derivatives is not greater than 12percent.
