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(3aR,4R,6R,6aS)-4-Benzoyl-6-naphthalen-1-yl-tehydrotra-furo[3,4-c]furan-1,3-dione is a complex organic compound with a unique molecular structure. It is characterized by a tetrahydrofuro[3,4-c]furan-1,3-dione core, which is a type of furan derivative with a four-membered ring containing an oxygen atom and a carbonyl group. The compound features a benzoyl group attached to the 4-position, which is an aromaticyl ac group derived from benzoic acid. Additionally, it has a naphthalen-1-yl group at the 6-position, indicating the presence of a naphthalene ring system. The stereochemistry of the compound is defined by the (3aR,4R,6R,6aS) configuration, which specifies the spatial arrangement of the atoms at these positions. (3aR,4R,6R,6aS)-4-Benzoyl-6-naphthalen-1-yl-tetrahydro-furo[3,4-c]furan-1,3-dione is likely to be of interest in the field of organic chemistry, potentially for its pharmacological properties or as a building block in the synthesis of more complex molecules.

73354-58-2

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73354-58-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73354-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,3,5 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73354-58:
(7*7)+(6*3)+(5*3)+(4*5)+(3*4)+(2*5)+(1*8)=132
132 % 10 = 2
So 73354-58-2 is a valid CAS Registry Number.

73354-58-2Relevant academic research and scientific papers

Photochimie d'α-epoxycetones. Reactions d'additions d'ylures intermediaires sur divers dipolarophiles

Hallet, Philippe,Muzart, Jacques,Pete, Jean-Pierre

, p. 262 - 264 (2007/10/02)

Ylides generated by photolysis of α-epoxyketones are trapped by bipolarophiles.A disrotatory opening of oxiran and a stereospecific cycloaddition are involved.

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