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  2. Tolyl group - Wikipedia

    en.wikipedia.org/wiki/Tolyl_group

    Structures of the three isomers of tolyl group. In organic chemistry, tolyl groups are functional groups related to toluene. [1] They have the general formula CH 3 C 6 H 4 −R, the change of the relative position of the methyl and the R substituent on the aromatic ring can generate three possible structural isomers 1,2 (ortho), 1,3 (meta), and 1,4 (para).

  3. Acetanisole - Wikipedia

    en.wikipedia.org/wiki/Acetanisole

    Acetanisole is an aromatic chemical compound with an aroma described as sweet, fruity, nutty, and similar to vanilla. In addition acetanisole can sometimes smell like butter or caramel. [3]

  4. Anisole - Wikipedia

    en.wikipedia.org/wiki/Anisole

    CH 3 OC 6 H 5 + (CH 3 CO) 2 O → CH 3 OC 6 H 4 C(O)CH 3 + CH 3 CO 2 H. Unlike most acetophenones, but reflecting the influence of the methoxy group, methoxyacetophenone undergoes a second acetylation. Many related reactions have been demonstrated. For example, phosphorus pentasulfide (P 4 S 10) converts anisole to Lawesson's reagent, [(CH 3 OC ...

  5. Phenol ether - Wikipedia

    en.wikipedia.org/wiki/Phenol_ether

    Anisole (C 6 H 5 OCH 3) is the simplest phenol ether, and is a versatile precursor for perfumes and pharmaceuticals. [1] Vanillin and ethylvanillin are phenol ether derivatives commonly utilized in vanilla flavorings and fragrances, while diphenyl ether is commonly used as a synthetic geranium fragrance.

  6. Category:4-Tolyl compounds - Wikipedia

    en.wikipedia.org/wiki/Category:4-Tolyl_compounds

    Pages in category "4-Tolyl compounds" The following 25 pages are in this category, out of 25 total. This list may not reflect recent changes. A. Acrivastine; B.

  7. 2,4-Dinitroanisole - Wikipedia

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

    2,4-Dinitroanisole (DNAN) is a low sensitivity organic compound. It has an anisole (methoxybenzene) core, with two nitro groups (–NO 2) attached. [1] It is not explosive itself unless it is mixed with other explosive chemicals in certain ratios. Compared with TNT it has only 90% of the explosive power and is less dense with a higher melting ...

  8. Tosyl group - Wikipedia

    en.wikipedia.org/wiki/Tosyl_group

    In organic chemistry, a toluenesulfonyl group (tosyl group, abbreviated Ts or Tos [nb 1]) is a univalent functional group with the chemical formula −SO 2 −C 6 H 4 −CH 3. It consists of a tolyl group, −C 6 H 4 −CH 3, joined to a sulfonyl group, −SO 2 −, with the open valence on sulfur. This group is usually derived from the ...

  9. Thioanisole - Wikipedia

    en.wikipedia.org/wiki/Thioanisole

    Thioanisole is an organic compound with the formula CH 3 SC 6 H 5.It is a colorless liquid that is soluble in organic solvents. It is the simplest alkyl–aryl thioether. The name indicates that this compound is the sulfur analogue—the thioether rather than the oxygen-centered ether—of anisole.

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