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(3aR,4R,6R,6aS)-4-Benzoyl-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 is a derivative of tetrahydrofuro[3,4-c]furan, a heterocyclic compound with a furan ring fused to a tetrahydrofuran ring. The molecule features a benzoyl group attached to the 4-position, a naphthalen-2-yl group at the 6-position, and a 1,3-dione functional group, indicating the presence of two carbonyl groups. This specific stereochemistry, with the 3aR, 4R, 6R, and 6aS configurations, influences its physical and chemical properties. Such compounds are often studied for their potential applications in pharmaceuticals, materials science, or as intermediates in organic synthesis, due to their diverse and intricate structures.

73354-59-3

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73354-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73354-59-3 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 73354-59:
(7*7)+(6*3)+(5*3)+(4*5)+(3*4)+(2*5)+(1*9)=133
133 % 10 = 3
So 73354-59-3 is a valid CAS Registry Number.

73354-59-3Relevant 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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