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5-Ethenyl-1,3-cyclohexadiene is an organic compound with the molecular formula C8H10. It is a conjugated diene, which means it contains two carbon-carbon double bonds separated by a single bond in a cyclic structure. The presence of the vinyl group (ethenyl) at the 5-position adds to its reactivity and chemical properties. 5-ethenyl-1,3-cyclohexadiene is known for its aromatic character and can participate in various chemical reactions, such as Diels-Alder reactions, due to its conjugated system. It is also used as an intermediate in the synthesis of other organic compounds and has applications in the pharmaceutical and chemical industries.

3725-32-4

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3725-32-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3725-32-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,2 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3725-32:
(6*3)+(5*7)+(4*2)+(3*5)+(2*3)+(1*2)=84
84 % 10 = 4
So 3725-32-4 is a valid CAS Registry Number.

3725-32-4Downstream Products

3725-32-4Relevant academic research and scientific papers

STRAINED CYCLOALKENYNES

Meier, Herbert,Hanold, Norbert,Molz, Thomas,Bissinger, Hans Joachim,Kolshorn, Heinz,Zountsas, Johannes

, p. 1711 - 1720 (2007/10/02)

Presently known strained cycloalkynes with one, two or three additional cis- or trans-configurated double bonds are summarized in Table 3.The main topics of the article are the geometrical ring strain, the preparation or in situ generation of these compounds by fragmentation of the corresponding 1,2,3-selendiazoles, and the thermal isomerisation processes performed at room temperature or in flash pyrolysis experiments at 440-640 deg C.

Synthesis and Characterization of Representative Octa-1,3,5,7-tetraenes and Deca-1,3,5,7,9-pentaenes

Spangler, Charles W.,Little, David A.

, p. 2379 - 2386 (2007/10/02)

Several representative conjugated linear tetraenes and pentaenes were prepared by a variety of synthetic methods including Wittig condensation, 1,8-Diazabicycloundec-7-ene (DBU)-induced dehydrobromination, and Hofmann elimination.For the preparation of (E,E)- and (Z,E)-octa-1,3,5,7-tetraene, the Hofmann elimination sequence is by far the most convenient method by synthesis, while DBU-induced dehydrobromination of (E,E)-4-bromonona-1,5,7-triene, produces excellent yields of (E,E,E)- and (3Z,5E,7E)-nona-1,3,5,7-tetraene.Deca-1,3,5,7,9-pentaene can be produced by several methods, but not in high yield.Undeca-1,3,5,7,9-pentaene and trideca-1,3,5,7,9,11-hexaene can also be prepared in low yield by the Wittig reaction.All the polyenes produced in this study polymerize rapidly in the crystalline state.

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