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1,2,4-Oxadiazole-3-carboxamide,5-[(aminoiminomethyl)amino]-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

519186-95-9

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519186-95-9 Usage

Explanation

The molecular formula represents the number of carbon (C), hydrogen (H), nitrogen (N), and oxygen (O) atoms in the compound.

Explanation

It belongs to a class of heterocyclic compounds with a five-membered ring containing two nitrogen atoms and one oxygen atom.

Explanation

The compound has a specific arrangement of functional groups, including an aminoiminomethylamino (-NH-NH-CH2-) group and a phenyl ring (C6H5) attached to the oxadiazole core.

Explanation

Due to its unique chemical structure and potential biological activities, the compound may be useful in the development of new drugs.

Explanation

The compound's specific functional groups and structure suggest that it may have interesting biological properties, which could be explored for therapeutic applications.

Explanation

The compound's properties and potential uses make it a promising candidate for further research and development in the pharmaceutical industry.

Explanation

The solubility of the compound is not provided, but it can be inferred that it may be influenced by the polarity of the solvent and the compound's functional groups.

Explanation

The stability of the compound is not provided, but it can be inferred that factors such as temperature, light, and humidity may affect its stability.

Explanation

The synthesis method for this specific compound is not mentioned in the material provided, but it can be inferred that it may involve the formation of the oxadiazole core and subsequent functionalization with the aminoiminomethylamino and phenyl groups.

Explanation

The reactivity of the compound is not provided, but it can be inferred that the presence of various functional groups, such as the amino and imino groups, may influence its reactivity with other compounds or reagents.

Type of compound

Oxadiazole derivative

Structural features

Contains an aminoiminomethylamino group and a phenyl group

Potential applications

Pharmaceutical industry

Biological activities

Unknown, but potentially significant

Research and development

Intriguing compound

Solubility

Unknown, but may vary depending on solvent

Stability

Unknown, but may be influenced by environmental factors

Synthesis

Not provided in the material

Reactivity

Unknown, but may be influenced by functional groups

Check Digit Verification of cas no

The CAS Registry Mumber 519186-95-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,9,1,8 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 519186-95:
(8*5)+(7*1)+(6*9)+(5*1)+(4*8)+(3*6)+(2*9)+(1*5)=179
179 % 10 = 9
So 519186-95-9 is a valid CAS Registry Number.

519186-95-9Downstream Products

519186-95-9Relevant academic research and scientific papers

Synthesis of 3-carbamoyl-1,2,4-oxadiazoles

Yarovenko,Kosarev,Zavarzin,Krayushkin

, p. 1857 - 1861 (2007/10/03)

A convenient method for the synthesis of 3-carbamoyl-1,2,4-oxadiazoles from carbamoylamidoximes and chlorides or anhydrides of haloacetic acids was developed. The reactions of 3-carbamoyl-5-trichloromethyl-1,2,4-oxadiazoles with amines and N,N-dimethylhydrazine were studied.

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