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  2. Toluene - Wikipedia

    en.wikipedia.org/wiki/Toluene

    As such, its systematic IUPAC name is methylbenzene. Toluene is predominantly used as an industrial feedstock and a solvent. As the solvent in some types of paint thinner, permanent markers, contact cement and certain types of glue, toluene is sometimes used as a recreational inhalant [16] and has the potential of causing severe neurological ...

  3. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    IUPAC nomenclature of organic chemistry. In chemical nomenclature, the IUPAC nomenclature of organic chemistry is a method of naming organic chemical compounds as recommended [1][2] by the International Union of Pure and Applied Chemistry (IUPAC). It is published in the Nomenclature of Organic Chemistry (informally called the Blue Book). [3]

  4. Chlorotoluene - Wikipedia

    en.wikipedia.org/wiki/Chlorotoluene

    Chlorotoluene. Chlorotoluenes are aryl chlorides based on toluene in which at least one aromatic hydrogen atom is replaced with a chlorine atom. They have the general formula C 7 H 8–n Cl n, where n = 1–5 is the number of chlorine atoms.

  5. Toluene (data page) - Wikipedia

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

    Structure and properties ... Physical and Chemical Properties of Toluene in chemeo.com This page was last edited on 12 April 2023, at 11:55 (UTC). ...

  6. 4-Ethyltoluene - Wikipedia

    en.wikipedia.org/wiki/4-Ethyltoluene

    4-Ethyltoluene is an organic compound with the formula CH 3 C 6 H 4 C 2 H 5. It is one of three isomers of ethyltoluene, the other two isomers being 3-ethyltoluene and 2-ethyltoluene. All are colorless liquids and all are used for the production of specialty polystyrenes.

  7. Benzyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloride

    Benzyl chloride is an alkylating agent. Indicative of its high reactivity (relative to alkyl chlorides), benzyl chloride slowly reacts with water in a hydrolysis reaction to form benzyl alcohol and hydrochloric acid. In contact with mucous membranes, hydrolysis produces hydrochloric acid. Thus, benzyl chloride is a lachrymator and has been used ...

  8. Butylated hydroxytoluene - Wikipedia

    en.wikipedia.org/wiki/Butylated_hydroxytoluene

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ?) 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]

  9. Benzal chloride - Wikipedia

    en.wikipedia.org/wiki/Benzal_chloride

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ?) Benzal chloride is an organic compound with the formula C 6 H 5 CHCl 2. [1] This colourless liquid is a lachrymator and is used as a building block in organic synthesis.