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Bicyclo(4.2.0)oct-7-ene is a bicyclic hydrocarbon compound with the molecular formula C8H12. It features a unique structure consisting of two carbon rings, one with four carbon atoms and the other with three, connected at a single carbon atom. This arrangement results in a strained molecule due to the presence of a quaternary carbon center and a trans-decalin system. The compound is known for its distinct chemical properties, such as its reactivity and potential applications in organic synthesis. Bicyclo(4.2.0)oct-7-ene is an example of a bridged bicyclic compound, which can be found in various natural products and has been studied for its potential use in the synthesis of complex organic molecules.

3806-82-4

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3806-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3806-82-4 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 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3806-82:
(6*3)+(5*8)+(4*0)+(3*6)+(2*8)+(1*2)=94
94 % 10 = 4
So 3806-82-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H12/c1-2-4-8-6-5-7(8)3-1/h5-8H,1-4H2

3806-82-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Bicyclo(4.2.0)oct-7-ene

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:3806-82-4 SDS

3806-82-4Relevant academic research and scientific papers

Photochemistry of Alkyl Halides. 10. Vinyl Halides and Vinylidene Dihalides

Kropp, Paul J.,McNeely, Steven A.,Davis, Robert Drummond

, p. 6907 - 6915 (2007/10/02)

The photobehavior of the acyclic vinyl iodide 2, the 1-iodocycloalkenes 11-14 and 39, the (halomethylene)cycloalkanes 45-48, and the (dihalomethylene)cyclohexanes 62-64 has been studied.Except for the dichloride 64, which exhibited only radical behavior, each of the halides afforded a mixture of ionic and radical products.The two bromides studied, 48 and 63, afforded lower ratios of ionic to radical products than the corresponding iodides 45 and 62.Irradiation of vinyl iodides was found to be a convenient and powerful method for the generation of vinyl cations, including the highly strained 1-cyclohexenyl and 1-cyclopentenyl cations and the unstabilized α-unsubstituted cations 51 and 54.The latter cations underwent rearrangement to the ring-expanded 1-cycloalkenyl cations 28 and 36, respectively.Lowering the temperature of the irradiation of iodides 13, 14, and 45 resulted in an increased ratio of ionic to radical products.However, iodide 47, which underwent principally fragmentation to enyne 61, showed little temperature effect.

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