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3-Nitro-5-phenylisoxazole is a chemical compound with the molecular formula C9H6N2O3. It is a derivative of isoxazole, a heterocyclic organic compound consisting of a five-membered ring with one oxygen and one nitrogen atom. The 3-nitro group refers to the presence of a nitro functional group (-NO2) at the 3rd position of the isoxazole ring, while the 5-phenyl group indicates a phenyl ring (C6H5) attached at the 5th position. 3-nitro-5-phenylisoxazole is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in organic chemistry. Due to its reactivity and functional groups, 3-nitro-5-phenylisoxazole can undergo further chemical reactions, making it a valuable building block in the development of new compounds with specific properties.

6455-30-7

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6455-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6455-30-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,5 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6455-30:
(6*6)+(5*4)+(4*5)+(3*5)+(2*3)+(1*0)=97
97 % 10 = 7
So 6455-30-7 is a valid CAS Registry Number.

6455-30-7Relevant academic research and scientific papers

Dinitrofuroxan cycloreversion as a novel general approach for the synthesis of nitroazoles

Fershtat,Khakimov,Makhova

, p. 415 - 422 (2015)

A novel general approach towards various nitroazoles via tandem process involving dinitrofuroxan cycloreversion followed by [3+2] cycloaddition of generated in situ nitroformonitrile oxide is developed. The reaction is promoted by addition of catalytic am

Ionic liquid-promoted [3+2]-cycloaddition reactions of nitroformonitrile oxide generated by the cycloreversion of dinitrofuroxan

Fershtat, Leonid L.,Ovchinnikov, Igor V.,Makhova, Nina N.

supporting information, p. 2398 - 2400 (2014/05/06)

A new approach to the synthesis of 3-nitroisoxazoles and 3-nitroisoxazolines based on the [3+2]-cycloaddition of nitroformonitrile oxide (NFNO), generated by the cycloreversion of dinitrofuroxan (DNFO), to acetylene and ethylene derivatives, under ionic liquid catalysis is developed. The approach is of a general nature and applicable to cycloaddition reactions with other dipolarophiles.

3-NITROISOXAZOLES AND THEIR USE IN THE PROTECTION OF MATERIALS

-

, (2012/09/11)

The 3-nitroisoxazoles of the formula (I) in which R1 and R2 are each as defined in the description, some of which are known, are highly suitable for use as biocides for protecting industrial materials.

Reaction of propargyl bromides with silver and sodium nitrites. A new method for the synthesis of nitroisoxazoles

Mechkov, Ts. D.,Sulimov, I. G.,Usik, N. V.,Mladenov, I.,Perekalin, V. V.

, p. 1148 - 1150 (2007/10/02)

The reaction of primary and secondary propargyl bromides with silver and sodium nitrites was investigated for the first time.In contrast to alkyl and allyl halides, the reaction does not stop at the stage of the formation of the normal mononitro compounds for the Meyer - Kornblum reaction and results in the synthesis of derivatives of 3- or 4-nitroisoxazoles.

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