5456-93-9 Usage
Uses
Used in Pharmaceutical Industry:
(5Z)-5-imino-4-[(4-methoxyphenyl)hydrazono]-1-phenyl-4,5-dihydro-1H-pyrazol-3-amine is used as a potential pharmaceutical candidate for various applications due to its structural features and potential biological activities. (5Z)-5-imino-4-[(4-methoxyphenyl)hydrazono]-1-phenyl-4,5-dihydro-1H-pyrazol-3-amine's imino and hydrazono groups, along with the pyrazole and phenyl rings, may contribute to its effectiveness in targeting specific biological pathways or receptors.
Used in Chemical Research:
In the field of chemical research, (5Z)-5-imino-4-[(4-methoxyphenyl)hydrazono]-1-phenyl-4,5-dihydro-1H-pyrazol-3-amine serves as a subject for further investigation to explore its properties, reactivity, and potential applications in the synthesis of other compounds or materials. Understanding its behavior in different reaction conditions can lead to the development of new methodologies or products.
Used in Material Science:
(5Z)-5-imino-4-[(4-methoxyphenyl)hydrazono]-1-phenyl-4,5-dihydro-1H-pyrazol-3-amine may also find applications in material science, particularly in the development of new materials with specific properties. Its unique structure could potentially be utilized in the creation of novel polymers, coatings, or other advanced materials with tailored characteristics for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5456-93-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5456-93:
(6*5)+(5*4)+(4*5)+(3*6)+(2*9)+(1*3)=109
109 % 10 = 9
So 5456-93-9 is a valid CAS Registry Number.
5456-93-9Relevant academic research and scientific papers
Sener, Nesrin,Sener, Izzet,Yavuz, Serkan,Karci, Fikret
, p. 3003 - 3012 (2015)
In this study, 20 novel disazo dyes containing pyrazole derivatives were synthesized by a convenient method. Diazotized aniline and some aniline derivatives were reacted with malononitrile to give 2-arylazomalononitrile derivatives 1(a-e). The synthesized 2-arylazomalononitrile derivatives were reacted with hydrazine and phenyl hydrazine to afford the corresponding 3,5-diamino-4-arylazo-1 H-pyrazole 2(a-e) and 3,5-diamino-4-arylazo-1-phenylpyrazole 3(a-e). Diazotized compounds of 2(a-e)and 3(a-e) reacted with ethylacetoacetate to give 4-arylazo-3-amino-1 H-pyrazole-5-ylazo-ethylacetoacetate 4(a-e) and 4-arylazo-3-amino-1-phenylpyrazole-5-ylazo-ethylacetoacetate 7(ae). The obtained 4(a-e) and 7(a-e) were reacted with hydrazine and phenyl hydrazine to give disazo dyes 5(a-e), 6(a-e), 8(a-e) and 9(a-e), respectively. The synthesized disazo dyes were characterized by spectroscopic techniques as well as elemental analysis. The solvatochromic behaviours of these dyes in various solvents were examined. Acid-base effects on the absorption maxima of the dyes were also reported. Antimicrobial activities of the synthesized novel disazo dyes were investigated.
