58668-41-0 Usage
Uses
Used in Plastics and Polymers Industry:
N'-(4-Formyl-3-methyl-1-phenyl-1H-pyrazol-5-yl)-N,N-dimethyliminoformamide is used as a chemical intermediate for the synthesis of various polymers and plastics. Its unique formamidine functional group contributes to the development of new materials with specific properties.
Used in Pharmaceutical Industry:
N'-(4-Formyl-3-methyl-1-phenyl-1H-pyrazol-5-yl)-N,N-dimethyliminoformamide is used as a building block in the synthesis of pharmaceutical compounds. Its potential applications in drug development are still under investigation, but its presence in the formamidines family suggests it may have therapeutic properties.
Used in Pesticides Industry:
N'-(4-Formyl-3-methyl-1-phenyl-1H-pyrazol-5-yl)-N,N-dimethyliminoformamide is used as a component in the formulation of certain pesticides. Its role in these products is to enhance their effectiveness against pests and insects.
Note: Due to the limited information available on N'-(4-Formyl-3-methyl-1-phenyl-1H-pyrazol-5-yl)-N,N-dimethyliminoformamide, the above uses are based on the general applications of formamidines. More research is needed to fully understand the chemical properties and potential applications of this specific compound. Caution must be exercised while handling formamidines as they may pose potential health hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 58668-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,6 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 58668-41:
(7*5)+(6*8)+(5*6)+(4*6)+(3*8)+(2*4)+(1*1)=170
170 % 10 = 0
So 58668-41-0 is a valid CAS Registry Number.
58668-41-0Relevant academic research and scientific papers
VILSMEIER-HAACK REACTION OF 5-AMINO- AND 5-ACYLAMINO-PYRAZOLES
Simay, A.,Takacs, K.,Horvath, K.,Dvortsak, P.
, p. 127 - 140 (2007/10/02)
The Vilsmeier-Haack reaction of 5-aminopyrazole derivatives 1 was investigated in view of contradictory literature reports.Structure 2 of the products was proved both chemically and spectroscopically.The mechanism of the reaction was postulated on the basis of isolated intermediates 7 and 8. 5-Acylaminopyrazoles 9, 10 and 11 were found to give also 2 (and 7) under the Vilsmeier conditions by an acyl splitting reaction, proceeding probably via diacylamino derivatives 12.Compounds 2 provided a simple route to pyrazolopyrimidine derivatives 13 and 14 as well as to azomethine compounds 15-18.