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3-(3-nitrophenyl)benzo[d]isoxazole is a chemical compound characterized by its unique molecular structure, which consists of a benzo[d]isoxazole ring system fused with a nitrophenyl group. 3-(3-nitrophenyl)benzo[d]isoxazole is notable for its potential applications in various fields, such as pharmaceuticals and materials science, where its specific properties may be harnessed for therapeutic or technological purposes. The presence of the nitro group on the phenyl ring introduces a distinct electronic and steric influence, which can significantly affect the compound's reactivity and interactions with other molecules. This makes 3-(3-nitrophenyl)benzo[d]isoxazole an interesting subject for chemical research and development, as its properties can be fine-tuned for specific applications through modifications to its structure.

7007-66-1

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7007-66-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7007-66-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,0 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7007-66:
(6*7)+(5*0)+(4*0)+(3*7)+(2*6)+(1*6)=81
81 % 10 = 1
So 7007-66-1 is a valid CAS Registry Number.

7007-66-1Downstream Products

7007-66-1Relevant academic research and scientific papers

Synthesis of benzisoxazoles by the [3 + 2] cycloaddition of in situ generated nitrile oxides and arynes

Dubrovskiy, Anton V.,Larock, Richard C.

supporting information; experimental part, p. 1180 - 1183 (2010/05/02)

"Chemical Equation Presented" A variety of substituted benzisoxazoles has been prepared by the [3 + 2] cycloaddition of nitrile oxides and arynes. Both components, being highly reactive intermediates, have been generated in situ by fluoride anion from readily prepared aryne precursors and chlorooximes, The reaction scope is quite general, affording a novel, direct route to functionalized benzisoxazoles under mild reaction conditions

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