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1,2,4-Oxadiazol-5-amine, 3-(4-methylphenyl)-, also known as 3-(4-Methylphenyl)-1,2,4-oxadiazol-5-amine, is a chemical compound with the molecular formula C8H8N3O2. It is a derivative of 1,2,4-oxadiazole, a five-membered heterocyclic ring containing two nitrogen atoms and one oxygen atom. The compound features a 4-methylphenyl group attached to the 3-position of the oxadiazole ring, which imparts unique chemical and physical properties. 1,2,4-Oxadiazol-5-amine, 3-(4-methylphenyl)- is often used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its versatile reactivity and stability.

3663-38-5

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3663-38-5 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 9 carbon (C), 9 hydrogen (H), 3 nitrogen (N), and 1 oxygen (O) atoms.

Explanation

The compound belongs to the oxadiazole class of compounds, which are characterized by a five-membered ring containing two nitrogen atoms and one oxygen atom.

Explanation

Due to its unique structure and potential for interaction with biological targets, 1,2,4-Oxadiazol-5-amine, 3-(4-methylphenyl)has potential uses in various fields, including the development of new drugs, agrochemicals, and materials.

Explanation

The compound's structure allows it to potentially interact with specific biological targets, making it a candidate for the development of new drugs or therapies.

Explanation

The compound's unique properties may contribute to the development of new materials with specific characteristics, such as improved stability or reactivity.

Explanation

The compound can be used as a building block or intermediate in the synthesis of more complex organic molecules, which may have various applications in different fields.

Explanation

Due to its diverse potential applications and unique properties, 1,2,4-Oxadiazol-5-amine, 3-(4-methylphenyl)is a subject of interest for researchers in fields such as chemistry, biology, and materials science.

Class

Oxadiazole

Applications

Pharmaceuticals, Agrochemicals, and Materials Science

Potential in Medicinal Chemistry

Interaction with Biological Targets

Applications in Material Science

Development of New Materials

Applications in Organic Synthesis

Synthesis of Complex Molecules

Research Interest

Various Scientific Disciplines

Check Digit Verification of cas no

The CAS Registry Mumber 3663-38-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,6 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3663-38:
(6*3)+(5*6)+(4*6)+(3*3)+(2*3)+(1*8)=95
95 % 10 = 5
So 3663-38-5 is a valid CAS Registry Number.

3663-38-5Downstream Products

3663-38-5Relevant academic research and scientific papers

SYNTHESIS AND THERMOLYSIS OF SOME N-HYDROXIMOYL- AND N-HYDRAZONOYLAZOLES

Plenkiewicz, Jan,Zdrojewski, Tadeusz

, p. 675 - 710 (2007/10/02)

The reactions of nitrile oxides or nitrile imines with pyrazole, imidazole, 1,2,3- and 1,2,4-triazole or tetrazole derivatives yield the appropriate N-hydroximoyl- or N-hydrazonoylazoles.Thermolysis of 1-hydroximoyltetrazoles, depending on the nature of the substituents in the tetrazole ring, yields 1,2,4-oxadiazoles or 5-amino-1,2,4-oxadiazoles upon hydrazoic acid or nitrogen evolution.Under similar conditions, 1-hydrazonoyltetrazoles give 1,2,4-triazoles or 5-amino-1,2,4-triazoles while 2-hydrazonoyltetrazoles decompose to the dihydro-1,2,4,5-tetrazine derivatives.

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