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1,3a-Dihydropentalene is a bicyclic organic compound with the molecular formula C7H10. It features a unique structure consisting of a cyclopentane ring fused to a cyclopropane ring, with the cyclopropane ring being part of a cyclohexane system. 1,3a-dihydropentalene is of interest in organic chemistry due to its strained ring system, which can lead to interesting chemical reactivity and potential applications in the synthesis of more complex molecules. The name "1,3a-dihydropentalene" reflects its relationship to pentalene, a hypothetical parent hydrocarbon, with the "1,3a-dihydro" prefix indicating the presence of two additional hydrogen atoms, one at each end of the molecule, which reduces the degree of unsaturation compared to pentalene.

75759-55-6

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75759-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75759-55-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,5 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75759-55:
(7*7)+(6*5)+(5*7)+(4*5)+(3*9)+(2*5)+(1*5)=176
176 % 10 = 6
So 75759-55-6 is a valid CAS Registry Number.

75759-55-6Downstream Products

75759-55-6Relevant academic research and scientific papers

Ein effizienter Zugang zu 1,5-Dihydropentalen und 2-Methyl-1,5-dihydropentalen aus Acrolein und Methacrolein

Griesbeck, Axel G.

, p. 144 - 147 (2007/10/02)

Acrolein and methacrolein can be converted into 1,5-dihydropentalene and its 2-methyl derivative, respectively, by a simple, three-step process. Cycloaddition of the aldehydes with cyclopentadiene affords 5-formyl-2-norbornenes which readily undergo condensation with cyclopentadiene to give 5-(cyclopentadienylidenemethyl)-2-norbornenes.These protected 6-vinylpentafulvenes undergo retro-cleave to cyclopentadiene and the 1,5-dihydropentalenes on vacuum flash thermolysis.

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