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  2. Toluene - Wikipedia

    en.wikipedia.org/wiki/Toluene

    Toluene (/ ˈ t ɒ l. j u iː n /), also known as toluol (/ ˈ t ɒ l. j u. ɒ l , - ɔː l , - oʊ l / ), is a substituted aromatic hydrocarbon [ 15 ] with the chemical formula C 6 H 5 CH 3 , often abbreviated as PhCH 3 , where Ph stands for the phenyl group.

  3. Toluene (data page) - Wikipedia

    en.wikipedia.org/wiki/Toluene_(data_page)

    Physical and Chemical Properties of Toluene in chemeo.com This page was last edited on 12 April 2023, at 11:55 (UTC). Text is available under the Creative Commons ...

  4. Toluene diisocyanate - Wikipedia

    en.wikipedia.org/wiki/Toluene_diisocyanate

    Toluene diisocyanate (TDI) is an organic compound with the formula CH 3 C 6 H 3 (NCO) 2.Two of the six possible isomers are commercially important: 2,4-TDI (CAS: 584-84-9) and 2,6-TDI (CAS: 91-08-7). 2,4-TDI is produced in the pure state, but TDI is often marketed as 80/20 and 65/35 mixtures of the 2,4 and 2,6 isomers respectively.

  5. Butylated hydroxytoluene - Wikipedia

    en.wikipedia.org/wiki/Butylated_hydroxytoluene

    Butylated hydroxytoluene (BHT), also known as dibutylhydroxytoluene, is a lipophilic organic compound, chemically a derivative of phenol, that is useful for its antioxidant properties. [7]

  6. Trifluorotoluene - Wikipedia

    en.wikipedia.org/wiki/Trifluorotoluene

    According to Ogawa and Curran, trifluorotoluene is similar to dichloromethane in standard acylation, tosylation, and silylation reactions. [4] The dielectric constants for dichloromethane and trifluorotoluene are 9.04 and 9.18, respectively, indicating similar solvating properties.

  7. 4-Ethyltoluene - Wikipedia

    en.wikipedia.org/wiki/4-Ethyltoluene

    Ethyltoluene is produced by ethylation of toluene: CH 3 C 6 H 5 + C 2 H 4 → CH 3 C 6 H 4 C 2 H 5. Over typical acid catalysts, this process gives a mixture of the 2-, 3-, and 4- isomers. Using a modified zeolite catalyst, the alkylation is shape-selective for the 4- isomer. [1] 4-Ethyltoluene is subjected dehydrogenation to give 4 ...

  8. 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.

  9. Diethyl toluene diamine - Wikipedia

    en.wikipedia.org/wiki/Diethyl_toluene_diamine

    Diethyl toluene diamine (DETDA) is a liquid aromatic organic molecule [2] with formula C 11 H 18 N 2. It is chemically an aromatic diamine and has the CAS Registry number of 68479-98-1. It has more than one isomer and the mixture of the two main isomers is given a different CAS number of 75389-89-8. [3]