enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Bromotoluene - Wikipedia

    en.wikipedia.org/wiki/Bromotoluene

    1-bromo-2-methylbenzene 1-bromo-3-methylbenzene 1-bromo-4-methylbenzene Molecular formula: C 7 H 7 Br (C 6 H 4 BrCH 3) Molar mass: 171.03 g/mol Appearance colorless liquid colorless liquid white crystalline solid CAS number [95-46-5] [591-17-3] [106-38-7] Properties Density and phase: 1.431 g/ml, liquid 1.4099 g/ml, liquid 1.3995 g/ml, solid ...

  3. o-Toluidine - Wikipedia

    en.wikipedia.org/wiki/O-Toluidine

    o-Toluidine is produced industrially by nitration of toluene to give a mixture of nitrotoluenes, favoring the ortho isomer. This mixture is separated by distillation. 2-Nitrotoluene is hydrogenated to give o-toluidine. [2] The conversion of o-toluidine to the diazonium salt gives access to the 2-bromo, 2-cyano-, and 2-chlorotoluene derivatives.

  4. 3-Nitrotoluene - Wikipedia

    en.wikipedia.org/wiki/3-nitrotoluene

    3-Nitrotoluene or meta-nitrotoluene is an organic compound with the formula CH 3 C 6 H 4 NO 2. It is one of three isomers of nitrotoluene. A yellow liquid, it is used in the manufacture of meta-toluidine, which is an intermediate in the production of various dyes. [3]

  5. Category:Nitrotoluenes - Wikipedia

    en.wikipedia.org/wiki/Category:Nitrotoluenes

    M. Mononitrotoluene; N. 2-Nitrotoluene; 3-Nitrotoluene; 4-Nitrotoluene This page was last edited on 30 January 2024, at 19:32 (UTC). Text is available under the ...

  6. 4-Nitrotoluene - Wikipedia

    en.wikipedia.org/wiki/4-Nitrotoluene

    Together with other isomers, 4-nitrotoluene is prepared by nitration of toluene, [4] commonly using titanium(IV) nitrate. [5] It undergoes the reactions typical for nitrobenzene derivatives, e.g. hydrogenation gives p-toluidine. Oxidation of the methyl substituent of 4-nitrotoluene has been extensively investigated.

  7. Bartoli indole synthesis - Wikipedia

    en.wikipedia.org/wiki/Bartoli_indole_synthesis

    The reaction mechanism [8] of the Bartoli indole synthesis is illustrated below using o-nitrotoluene (1) and propenyl Grignard (2) to form 3,7-dimethylindole (13). The mechanism of the Bartoli indole synthesis. The mechanism begins by the addition of the Grignard reagent (2) onto the nitroarene (1) to form intermediate 3.

  8. Mononitrotoluene - Wikipedia

    en.wikipedia.org/wiki/Mononitrotoluene

    Mononitrotoluene or nitrotoluene (MNT or NT), is any of three organic compounds with the formula C 6 H 4 (CH 3)(NO 2). [1] They can be viewed as nitro derivatives of toluene or as methylated derivatives of nitrobenzene. Mononitrotoluene comes in three isomers, differing by the relative position of the methyl and nitro groups. All are pale ...

  9. 2-Nitrotoluene - Wikipedia

    en.wikipedia.org/wiki/2-nitrotoluene

    2-Nitrotoluene or ortho-nitrotoluene is an organic compound with the formula CH 3 C 6 H 4 NO 2. It is pale yellow liquid that crystallizes in two forms, called α (−9.27 °C) and β (−3.17 °C). It is mainly a precursor to o-toluidine, which is an intermediate in the production of various dyes. [4]