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  2. Cycloheptene - Wikipedia

    en.wikipedia.org/wiki/Cycloheptene

    Cycloheptene is a 7-membered cycloalkene with a flash point of −6.7 °C. It is a raw material in organic chemistry and a monomer in polymer synthesis. Cycloheptene can exist as either the cis- or the trans-isomer.

  3. Cyclohexanetetrol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanetetrol

    The synthesis of cyclohexanetetrols can be achieved by, among other methods: reduction or hydrogenation of (1) cyclohexenetetrols, (2) tri-hydroxycyclohexanones, (3) pentahydroxycyclohexanones, (4) hydroxylated aromatic hydrocarbons, or (5) hydroxylated quinones; the (6) hydrogenolysis of dibromocyclohexanetetrols; the (7) hydration of ...

  4. IUPAC numerical multiplier - Wikipedia

    en.wikipedia.org/wiki/IUPAC_numerical_multiplier

    2 di- 31 hentriaconta- 3 tri- 32 dotriaconta- 4 tetra- 33 tritriaconta- 5 penta- 34 tetratriaconta- 6 hexa- 40 tetraconta- 7 hepta- 50 pentaconta- 8 octa- 60 hexaconta- 9 nona- 70 heptaconta- 10 deca- 80 octaconta- 11 undeca- 90 nonaconta- 12 dodeca- 100 hecta- 13 trideca- 200 dicta- 14 tetradeca- 300 tricta- 15 pentadeca- 400 tetracta- 16

  5. Norbornene - Wikipedia

    en.wikipedia.org/wiki/Norbornene

    Norbornene is made by a Diels–Alder reaction of cyclopentadiene and ethylene.Many substituted norbornenes can be prepared similarly. [2] [3] Related bicyclic compounds are norbornadiene, which has the same carbon skeleton but with two double bonds, and norbornane which is prepared by hydrogenation of norbornene.

  6. Cyclohexene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexene

    Cyclohexene is produced by the partial hydrogenation of benzene, a process developed by the Asahi Chemical company. [4] The main product of the process is cyclohexane because cyclohexene is more easily hydrogenated than benzene. In the laboratory, it can be prepared by dehydration of cyclohexanol. [5] C 6 H 11 OH → C 6 H 10 + H 2 O

  7. 3,9-Diethylidene-2,4,8,10-tetraoxaspiro(5.5)undecane - Wikipedia

    en.wikipedia.org/wiki/3,9-Diethylidene-2,4,8,10...

    3,9-Diethylidene-2,4,8,10-tetraoxaspiro[5.5]undecane (DETOSU) is a bicyclic ketene acetal derived from the isomeric allyl acetal 3,9-divinyl-2,4,8,10-tetraoxaspiro[5.5]undecane (DVTOSU). As a bifunctional monomer, DETOSU is an important building block for polyorthoesters formed by the addition of diols to the activated double bond of the ...

  8. Tropone - Wikipedia

    en.wikipedia.org/wiki/Tropone

    Tropone or 2,4,6-cycloheptatrien-1-one is an organic compound with some importance in organic chemistry as a non-benzenoid aromatic. [2] The compound consists of a ring of seven carbon atoms with three conjugated alkene groups and a ketone group.

  9. Heptene - Wikipedia

    en.wikipedia.org/wiki/Heptene

    Heptene is a higher olefin, or alkene with the formula C 7 H 14. The commercial product is a liquid that is a mixture of isomers . It is used as an additive in lubricants, as a catalyst , and as a surfactant .