4320-83-6 Usage
Uses
Used in Pharmaceutical Industry:
4-Phenylisoxazol-5-amine is used as a building block for the synthesis of various organic molecules and drug candidates. Its unique structure and properties make it a valuable component in the development of new pharmaceuticals.
Used in Medicinal Chemistry Research:
4-Phenylisoxazol-5-amine is used as a starting material in the design and synthesis of novel compounds with potential pharmacological properties. It has been studied for its potential as an anti-inflammatory and analgesic agent, making it a promising candidate for the development of new medications to treat pain and inflammation.
Used in Chemical Biology Research:
4-Phenylisoxazol-5-amine serves as a valuable tool in chemical biology research, where it can be used to probe the interactions between small molecules and biological targets. Its unique structure allows for the investigation of various biological processes and the development of new therapeutic strategies.
Used in Material Science:
4-Phenylisoxazol-5-amine has been investigated for its potential application in the development of new materials. Its chemical properties and structural features make it a candidate for use in the creation of advanced materials with specific properties for various applications.
Safety Considerations:
It is important to handle and use 4-Phenylisoxazol-5-amine with care, as it may pose risks to human health and the environment. Proper safety measures should be taken during its synthesis, storage, and application to minimize potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 4320-83-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,2 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4320-83:
(6*4)+(5*3)+(4*2)+(3*0)+(2*8)+(1*3)=66
66 % 10 = 6
So 4320-83-6 is a valid CAS Registry Number.
4320-83-6Relevant academic research and scientific papers
PHARMACEUTICAL COMPOUND
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Page/Page column 92, (2016/03/14)
Provided is a tryptophan-2,3-dioxygenase (TDO) and/or indoleamine-2,3-dioxygenase (IDO) inhibitor compound for use in medicine, which compound comprises the following formula (I): wherein X1 is selected from C and N; X3 and X5/
Pulse Radiolysis Study of the Reduction of 1-Phenyl-1-cyanonitroethylene. Cyclization Leading to 5-Amino-4-phenylisoxazole
Deswarte, S.,Bellec, C.,Pucheault, J.,Ferradini, C.,Gilles, L.
, p. 891 - 896 (2007/10/02)
It is known that the electrochemical reduction of the 1-phenyl-1-cyanonitroethylene leads to the formation of a cyclic compound, the 5-amino-4-phenylisoxazole, but the mechanism of such a cyclization, which is pH dependent, is not clearly established.Pulse radiolytic methods were used to follow the various stages resulting from the reduction of 1-phenyl-1-cyanonitroethylene by the radical anion COO- in order to obtain a better understanding of the preceding reduction.The transient spectra are studied between 250 and 400 nm for times ranging from 4 microseconds to several minutes after pulse; one of these spectra concerns the ene hydroxylamine.As expected, the changes and evolution of the spectra are pH dependent and corresponding mechanism are proposed to explain the cyclization following the formation of the ene hydroxylamine.A general scheme is given taking into account all the results obtained.
