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(3aR,4R,6R,6aS)-4-(Naphthalene-2-carbonyl)-6-naphthalen-2-yl-tetrahydro-furo[3,4-c]furan-1,3-dione is a complex organic compound characterized by its unique molecular structure. It features a tetrahydrofuro[3,4-c]furan-1,3-dione core, which is a type of furan derivative with a saturated ring structure. The compound is further distinguished by the presence of a naphthalene-2-carbonyl group at the 4-position and a naphthalen-2-yl group at the 6-position, both of which are derived from naphthalene, a polycyclic aromatic hydrocarbon. The stereochemistry of the compound is defined by the (3aR,4R,6R,6aS) configuration, indicating the specific spatial arrangement of the atoms at these positions. (3aR,4R,6R,6aS)-4-(Naphthalene-2-carbonyl)-6-naphthalen-2-yl-tetrahydro-furo[3,4-c]furan-1,3-dione is likely to be found in specialized chemical research or pharmaceutical applications due to its intricate structure and potential for specific interactions with biological targets.

73354-60-6

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73354-60-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73354-60-6 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, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 73354-60:
(7*7)+(6*3)+(5*3)+(4*5)+(3*4)+(2*6)+(1*0)=126
126 % 10 = 6
So 73354-60-6 is a valid CAS Registry Number.

73354-60-6Downstream Products

73354-60-6Relevant 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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