4280-78-8 Usage
Uses
Used in Organic Synthesis:
3-AMINO-5-METHYL-1-PHENYLPYRAZOLE is used as a building block in organic synthesis for the preparation of various chemical compounds. Its unique structure allows for the formation of a wide range of derivatives, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In pharmaceutical research, 3-AMINO-5-METHYL-1-PHENYLPYRAZOLE is employed as a key intermediate for the development of new pharmaceutical compounds. Its potential pharmacological and biological activities, such as enzyme inhibition and antitumor properties, make it a promising candidate for the discovery of novel therapeutic agents.
Used in Enzyme Inhibition:
3-AMINO-5-METHYL-1-PHENYLPYRAZOLE has been investigated for its role as an inhibitor of certain enzymes. Its ability to modulate enzyme activity can be leveraged in the development of drugs targeting specific enzymatic pathways, offering potential therapeutic benefits in various diseases.
Used in Antitumor Applications:
As an antitumor agent, 3-AMINO-5-METHYL-1-PHENYLPYRAZOLE has shown potential in inhibiting the growth and progression of cancer cells. Its incorporation into drug development pipelines may lead to the creation of new cancer treatments, providing additional options for patients and healthcare professionals.
Used in Optoelectronic Applications:
3-AMINO-5-METHYL-1-PHENYLPYRAZOLE also exhibits potential for use in the development of materials for optoelectronic applications, such as light-emitting diodes (LEDs) and organic semiconductors. Its unique electronic properties make it a candidate for improving the performance and efficiency of these optoelectronic devices.
Used in the Optoelectronic Industry:
In the optoelectronic industry, 3-AMINO-5-METHYL-1-PHENYLPYRAZOLE is used as a material for the development of light-emitting diodes and organic semiconductors. Its electronic properties contribute to enhancing the performance and efficiency of these devices, driving innovation and advancements in optoelectronic technology.
Check Digit Verification of cas no
The CAS Registry Mumber 4280-78-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,8 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4280-78:
(6*4)+(5*2)+(4*8)+(3*0)+(2*7)+(1*8)=88
88 % 10 = 8
So 4280-78-8 is a valid CAS Registry Number.
4280-78-8Relevant academic research and scientific papers
Reactivity of α-acylated β-enamino ketones and esters: Synthesis of pyrazoles
Missio, Lauri J.,Braibante, Hugo S.,Braibante, Mara E. F.
, p. 1243 - 1245 (2007/10/03)
The reactivity of the enamino compounds 4-amino-3-phenylamino(thio)carbonyl-3-penten-2-one 1 and 2 and ethyl 3-amino-2-phenylamino(thio)carbonyl-2-butyrate 7 and 8 was studied using the reaction with hydrazine hydrate and hydrazine hydrochloride to evaluate the 1,3 electrophilic center of the compounds by the formation of the pyrazole rings. The pyrazoles 3,4,5,9,11 and 13 were obtained depending on the reaction conditions employed.
Pyrazole-3-amines as anti-inflammatory agents
-
, (2008/06/13)
There are described compounds of formula I, STR1 in which R1 represents hydrogen, alkyl, alkanoyl or alkyl substituted by Ar1, R3, R4 and R5, which may be the same or different, each independently rep
