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(1S,5R)-6-exo-acetyl-2-exo,3-endo-dibenzoyloxytricyclo[3.2.0.0^2,7^]heptane is a complex organic compound with a unique molecular structure. It is a tricyclic compound, which means it consists of three interconnected rings. The compound is characterized by its stereochemistry, with the 1S and 5R configurations indicating the spatial arrangement of the atoms at these positions. The molecule features an exo-acetyl group at the 6-position and two dibenzoyloxy groups at the 2-exo and 3-endo positions, which are ester derivatives of benzoic acid. These functional groups contribute to the compound's reactivity and potential applications in various chemical processes. The compound's structure and properties make it a subject of interest in organic chemistry, particularly in the study of complex molecular architectures and their synthesis.

88203-84-3

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88203-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88203-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,0 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88203-84:
(7*8)+(6*8)+(5*2)+(4*0)+(3*3)+(2*8)+(1*4)=143
143 % 10 = 3
So 88203-84-3 is a valid CAS Registry Number.

88203-84-3Relevant academic research and scientific papers

Functionalised Carbocycles from Carbohydrates. Part 4. The Synthesis of the Epoxy Lactone Prostaglandin Intermediate via Bicycloheptane Derivatives. X-Ray Crystal Structure of (1R)-5-endo-Acetyl-2-exo,3-endo-dibenzoyloxybicycloheptane

Ferrier, Robert J.,Prasit, Petpiboon,Gainsford, Graeme J.,Page, Yvonne Le

, p. 1635 - 1640 (2007/10/02)

Irradiation of the nona-3,8-dienulose derivative (2) at 350 nm gave the bicycloheptyl methyl ketone (3) in good yield.This was converted via the acetate (5) into the corresponding bicycloheptanol (6) which, with base, gave the cyclopentenyl aldehyd

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