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Hexahydro-2,6-methanooxireno[f][2]benzofuran-3,5-dione is a complex organic chemical compound with the molecular formula C10H10O4. It is a derivative of benzofuran, which is a heterocyclic aromatic organic compound consisting of a benzene ring fused to a furan ring. The compound's structure features a hexahydro-2,6-methano bridge, which connects two carbon atoms in the benzene ring, and an oxirene group, which is an epoxide ring. The molecule also contains two carbonyl groups at the 3 and 5 positions, which contribute to its reactivity and potential applications in various chemical reactions. Due to its unique structure, hexahydro-2,6-methanooxireno[f][2]benzofuran-3,5-dione may have potential applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals. However, further research and characterization are needed to fully understand its properties and potential uses.

6004-80-4

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6004-80-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6004-80-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,0 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6004-80:
(6*6)+(5*0)+(4*0)+(3*4)+(2*8)+(1*0)=64
64 % 10 = 4
So 6004-80-4 is a valid CAS Registry Number.

6004-80-4Relevant academic research and scientific papers

CHEMICAL REPERCUSSIONS OF ORBITAL INTERACTIONS THROUGH BOND AND THROUGH SPACE. EFFECT OF REMOTE SUBSTITUENTS ON THE ADDITION OF NITRENES TO BICYCLIC OLEFINS

Aitken, R. Alan,Gosney, Ian,Farries, Hugh,Palmer, Michael H.,Simpson, Isobel,et. al.

, p. 1329 - 1346 (2007/10/02)

The reactivity of a series of bicyclic olefins with nitrenes is profoundly influenced by the nature of remote functional groups.There is a marked lack of reactivity for reactions with carboethoxynitrene as compared to phthalimidonitrene which is distinctly nucleophilic in character.An explanation for the reluctance to form aziridines is offered in terms of orbital interactions between the distant groups and the olefinic bond, making the latter remarkably electron deficient as evidenced by UV-photoelectron spectroscopy.Because of the complexity of the spectra, identification of the Ip associated with the reactive ?-centre was made by recourse to ab initio configuration interaction calculations for key members of the series.

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