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  2. 1,4-Dicyanobenzene - Wikipedia

    en.wikipedia.org/wiki/1,4-Dicyanobenzene

    1,4-Dicyanobenzene is an organic compound with the formula C 6 H 4 (CN) 2. Two other isomers exist, phthalonitrile and isophthalonitrile. All three isomers are produced commercially by ammoxidation of the corresponding xylene isomers. 1,4-Dicyanobenzene is a colorless or white solid with low solubility in water. [1]

  3. Benzhydryl compounds - Wikipedia

    en.wikipedia.org/wiki/Benzhydryl_compounds

    This group typically excludes compounds in which either benzene is fused to another ring (bicyclic, tricyclic, polycyclic) [1] or includes a heteroatom, or where the methane connects to three or four benzenes. Ball-and-stick model of the benzhydryl radical. The benzhydryl radical can be abbreviated Ph 2 CH• or Bzh. [2]

  4. 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]

  5. Bis(2-ethylhexyl) terephthalate - Wikipedia

    en.wikipedia.org/wiki/Bis(2-ethylhexyl)_tere...

    Bis(2-ethylhexyl) terephthalate commonly abbreviated DEHT (Dioctyl terephthalate or DOTP), is an organic compound with the formula C 6 H 4 (CO 2 C 8 H 17) 2. It is a non- phthalate plasticizer , being the diester of terephthalic acid and the branched-chain 2-ethylhexanol , which is often generically referred to as octyl.

  6. Undecanol - Wikipedia

    en.wikipedia.org/wiki/Undecanol

    Undecanol, also known by its IUPAC name 1-undecanol or undecan-1-ol, and by its trivial names undecyl alcohol and hendecanol, is a fatty alcohol. Undecanol is a colorless, water-insoluble liquid of melting point 19 °C and boiling point 243 °C.

  7. Diethylbenzenes - Wikipedia

    en.wikipedia.org/wiki/Diethylbenzenes

    Diethylbenzenes arise as side-products of the alkylation of benzene with ethylene, which can be described as two steps. The first step is the industrial route to ethylbenzene, which is produced on a large scale as a precursor to styrene. C 6 H 6 + C 2 H 4 → C 6 H 5 C 2 H 5. The diethylbenzene is an inadvertent side product. C 6 H 5 C 2 H 5 ...

  8. Xylylene dichloride - Wikipedia

    en.wikipedia.org/wiki/Xylylene_dichloride

    The structure of xylylene dichloride is characterized by an benzene ring with two chloromethyl groups and four hydrogen atoms bound to it. [4] The chloromethyl groups can be located on different sites on the ring, leading to a few different possible forms. These forms are: [3] o-xylylene dichloride: 1,2-bis(chloromethyl)benzene

  9. Dibromobenzene - Wikipedia

    en.wikipedia.org/wiki/Dibromobenzene

    [108-36-1] [106-37-6] Properties Density and phase: 1.9940 g/ml, liquid 1.9523 g/ml, liquid 1.84 g/ml, solid Solubility in water: practically insoluble Other solubilities Soluble in 70 parts ethanol. Soluble in benzene, chloroform and very soluble in diethyl ether. Melting point: 7.1 °C −7.0 °C 87 °C Boiling point: 225 °C 218–220 °C ...