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6-iodo-7-methylhexahydro-2H-3,5-methanocyclopenta[b]furan-2-one is a complex organic compound with the molecular formula C8H13IO2. It features a hexahydro-3,5-methanocyclopenta[b]furan-2-one core structure, which is a type of cyclic ether with a methyl group (CH3) at the 7-position and an iodine atom (I) at the 6-position. 6-iodo-7-methylhexahydro-2H-3,5-methanocyclopenta[b]furan-2-one is characterized by its unique molecular structure, which includes a fused cyclopentane and cyclopropane ring system, and a carbonyl group (C=O) at the 2-position. Due to its specific functional groups and stereochemistry, it may have potential applications in various fields, such as pharmaceuticals or materials science, although its specific uses are not detailed in this summary.

26097-15-4

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26097-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26097-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,9 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26097-15:
(7*2)+(6*6)+(5*0)+(4*9)+(3*7)+(2*1)+(1*5)=114
114 % 10 = 4
So 26097-15-4 is a valid CAS Registry Number.

26097-15-4Relevant academic research and scientific papers

Hydrophobic effects are dominant over secondary orbital interactions for a simple Diets-Alder reaction in salt solutions

Sarma, Diganta,Kumar, Anil

, p. 2199 - 2202 (2007/10/03)

The stereoselectivity ratios for a Diels-Alder reaction between cyclopentadiene with methyl trans-crotonate carried out in salt solutions demonstrate the dominance of hydrophobic effects over secondary orbital interactions.

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