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(1S,5R)-2-exo,3-endo-dibenzoyloxy-6-oxo-4-exo-tosyloxybicyclo<3.2.0>heptane is a complex organic compound with a unique molecular structure. It consists of a bicyclo[3.2.0]heptane core, which is a seven-membered ring with two carbon atoms forming a bridge between two of the ring's vertices. The compound features a 6-oxo group, indicating the presence of a carbonyl group at the 6th position, and a 4-exo-tosyloxy group, which is a tosyloxy group (a sulfonate ester derived from toluenesulfonic acid) attached to the 4th position from the outside of the ring. Additionally, the molecule has two dibenzoyloxy groups, which are benzoyl esters of hydroxyl groups, located at the 2nd and 3rd positions. The stereochemistry of the compound is defined by the (1S,5R) configuration, indicating that the hydroxyl groups at the 1st and 5th positions are in the S and R configurations, respectively. (1S,5R)-2-exo,3-endo-dibenzoyloxy-6-oxo-4-exo-tosyloxybicyclo<3.2.0>heptane is likely to be found in the field of organic chemistry, particularly in the synthesis of complex molecules and pharmaceuticals, due to its intricate structure and potential reactivity.

88203-87-6

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88203-87-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88203-87-6 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 88203-87:
(7*8)+(6*8)+(5*2)+(4*0)+(3*3)+(2*8)+(1*7)=146
146 % 10 = 6
So 88203-87-6 is a valid CAS Registry Number.

88203-87-6Relevant 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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