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2,4-Pentadienyl, also known as 2,4-pentadien-1-yl, is an organic compound with the molecular formula C5H7. It is a conjugated diene, meaning it has two carbon-carbon double bonds separated by a single bond, which gives it unique chemical properties. This unsaturated hydrocarbon is a reactive intermediate often used in organic synthesis, particularly in the formation of various organic compounds through reactions such as Diels-Alder cycloadditions. The 2,4-pentadienyl group is characterized by its ability to participate in various chemical reactions due to the presence of the electron-rich double bonds, making it a valuable building block in the synthesis of complex organic molecules.

3808-35-3

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3808-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3808-35-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,0 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3808-35:
(6*3)+(5*8)+(4*0)+(3*8)+(2*3)+(1*5)=93
93 % 10 = 3
So 3808-35-3 is a valid CAS Registry Number.

3808-35-3Upstream product

3808-35-3Downstream Products

3808-35-3Relevant academic research and scientific papers

Dissociation of 3-Methylpenta-1,4-diene and the Resonance Energy of the Pentadienyl Radical

Trenwith, Antony B.

, p. 3131 - 3136 (2007/10/02)

From measurements of the initial rate of formation of methane in the pyrolysis of 3-methylpenta-1,4-diene at temperatures over the range 653-716 K and pressures between 15 and 200 Torr, methane has been shown to be formed by an homogeneous, first-order process.Examination of the other products of pyrolisis shows the most reasonable mode of formation of primary methane to be followed by .The rate expression for reaction (i) is where θ=2.303 RT/cal mol-1 (1 cal=4.18 J) and this leads to D=76.4 kcal mol-1, which by comparison with the value of 95.0 for the secondary C-H bond dissociation energy in alkanes leads to a figure of 18.6+/-1.5 kcal mol-1 for the resonance stabilisation energy of the pentadienyl radical.

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