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(Z,Z)-5-(cyclo-oct-4-enyl)cyclooctene is a complex organic compound with a molecular formula of C16H24. It is characterized by two cycloalkene rings, with one being a cyclooctene and the other a cyclooct-4-enyl group. The compound has a double bond configuration in both rings, with the Z,Z notation indicating that the substituents on each double bond are on the same side when viewed from the priority end of the bond. This geometric isomerism contributes to its unique chemical properties and potential applications in various fields, such as organic synthesis and materials science.

4103-14-4

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4103-14-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4103-14-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,0 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4103-14:
(6*4)+(5*1)+(4*0)+(3*3)+(2*1)+(1*4)=44
44 % 10 = 4
So 4103-14-4 is a valid CAS Registry Number.

4103-14-4Downstream Products

4103-14-4Relevant academic research and scientific papers

The cis-Cyclo-oct-4-enyl Radical is Reluctant to Rearrange

Bloodworth, A. J.,Crich, David,Melvin, T.

, p. 786 - 788 (1987)

The cis-cyclo-oct-4-enyl radical, generated both photochemically and thermally from the O-acyl thiohydroxamate (9) is efficiently trapped by (9), terachloromethane, 1,1-diethylpropanethiol, and oxygen.

Chemistry of the (Z)-Cyclo-oct-4-enyl Radical Including the Preparation of 18O2-Labelled (Z)-Cyclo-oct-4-enyl Hydroperoxide

Bloodworth, A. J.,Crich, David,Melvin, T.

, p. 2957 - 2961 (2007/10/02)

Photolysis of the O-acyl thiohydroxamate (2), precursor to the (Z)-cyclo-oct-4-enyl radical, in the presence of 18O2 and tertiary thiol provides the labelled hydroperoxide (8).The parent (Z)-cyclo-oct-4-enyl radical is shown to undergo transannular cyclization only under relatively forcing conditions.

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