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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. 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.

  4. 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

  5. 2,4-Dinitrophenylhydrazine - Wikipedia

    en.wikipedia.org/wiki/2,4-Dinitrophenylhydrazine

    Selected parameters: C=N, 128 pm; N-N, 1.38 pm, N-N-C(Ar), 119 [4] When 3-heptanone is added to a solution of 2,4-DNPH and heated, an orange-red precipitate forms. DNP-derived hydrazones have characteristic melting points, facilitating identification of the carbonyl. In particular, the use of DNPH was developed by Brady and Elsmie. [5]

  6. Dinitrobenzene - Wikipedia

    en.wikipedia.org/wiki/Dinitrobenzene

    The three possible arrangements of the nitro groups afford three isomers, 1,2-dinitrobenzene, 1,3-dinitrobenzene, and 1,4-dinitrobenzene. Each isomer has the chemical formula C 6 H 4 N 2 O 4 and a molar mass of about 168.11 g/mol. 1,3-Dinitrobenzene is the most common isomer and it is used in the manufacture of explosives .

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

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

    The diketene acetal 3,9-diethylidene-2,4,8,10-tetraoxaspiro[5.5]undecane, DETOSU, is a reactive bifunctional monomer that forms biodegradable polyorthoesters by polyaddition with α,ω-diols. Polyorthoesters are used as embedding media for pharmaceuticals in extended release formulations for controlled drug release by surface erosion under ...

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  9. Triazabicyclodecene - Wikipedia

    en.wikipedia.org/wiki/Triazabicyclodecene

    Triazabicyclodecene (1,5,7-triazabicyclo[4.4.0]dec-5-ene or TBD) is an organic compound consisting of a bicyclic guanidine. For a charge-neutral compound, it is a relatively strong base that is effective for a variety of organic transformations. TBD is colorless solid that is soluble in a variety of solvents. [4]