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4-Phenyl-3-furoxancarboxitrile is a chemical compound with the molecular formula C12H6N2O2. It is a derivative of furoxan, a heterocyclic compound containing a furan ring and an oxime group. This particular compound features a phenyl group attached to the furoxan ring, which imparts unique chemical and physical properties. It is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential applications, 4-phenyl-3-furoxancarboxitrile has been the subject of research in organic chemistry, with studies focusing on its synthesis, properties, and potential uses in various industries.

497-27-8

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497-27-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 497-27-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 497-27:
(5*4)+(4*9)+(3*7)+(2*2)+(1*7)=88
88 % 10 = 8
So 497-27-8 is a valid CAS Registry Number.

497-27-8Upstream product

497-27-8Downstream Products

497-27-8Relevant academic research and scientific papers

Oxidation of: O -dioxime by (diacetoxyiodo)benzene: Green and mild access to furoxans

He, Chunlin,Pang, Siping,Zhang, Qi,Zhang, Xun,Zhao, Cheng

supporting information, p. 1489 - 1493 (2022/01/31)

Furoxan has been widely used in the field of high energy density materials because of its excellent properties such as high density, high standard enthalpy of formation and high nitrogen content. However, its existing synthesis methods are still restricted by the problems of difficult substrate preparation and manual handling of hazardous reagents. Herein, we disclosed a mild oxidation strategy to efficiently obtain furoxan derivatives starting from readily available o-dioxime substrates. This reaction features high functional group tolerance and easy scale-up, and has excellent regioselectivity for specific nonsymmetric o-dioximes. This method greatly reduces the safety risk and simplifies the operation process, and means that diversified furoxan derivatives can be easily accessed, thus paving the way for the wide application of furoxan derivatives. This journal is

Synthesis method of furoxan compound

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Paragraph 0061-0068, (2021/01/04)

The invention discloses a synthesis method of a furazan oxide compound. The synthesis method comprises the following step of: oxidizing a glyoxime compound by taking iodobenzene diethyl ester as an oxidizing agent to carry out a reaction to obtain the fur

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