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  2. o-Anisic acid - Wikipedia

    en.wikipedia.org/wiki/O-Anisic_acid

    o-Anisic acid is an organic compound with the formula CH 3 OC 6 H 4 CO 2 H. A colorless solid, it is one of the isomers of anisic acid . The compound has been well studied with respect to intramolecular hydrogen bonding [ 2 ] and as a substrate for various catalystic reactions.

  3. Anisic acid - Wikipedia

    en.wikipedia.org/wiki/Anisic_acid

    Anisic acid or methoxybenzoic acid is an organic compound which is a carboxylic acid. It exists in three forms, depending on arene substitution patterns: p-Anisic acid (4-methoxybenzoic acid) m-Anisic acid (3-methoxybenzoic acid) o-Anisic acid (2-methoxybenzoic acid)

  4. C8H8O3 - Wikipedia

    en.wikipedia.org/wiki/C8H8O3

    The molecular formula C 8 H 8 O 3 (molar mass: 152.15 g/mol) may refer to: . Anisic acids. o-Anisic acid (2-methoxybenzoic acid); m-Anisic acid (3-methoxybenzoic acid); p-Anisic acid (4-methoxybenzoic acid)

  5. p-Anisic acid - Wikipedia

    en.wikipedia.org/wiki/P-Anisic_acid

    p-Anisic acid, also known as 4-methoxybenzoic acid or draconic acid, is one of the isomers of anisic acid. The term "anisic acid" often refers to this form specifically. [ 1 ] It is a white crystalline solid which is insoluble in water, highly soluble in alcohols, and soluble in ether and ethyl acetate .

  6. Dicamba - Wikipedia

    en.wikipedia.org/wiki/Dicamba

    Dicamba (3,6-dichloro-2-methoxybenzoic acid) is a selective systemic herbicide first registered in 1967. [4] Brand names for formulations of this herbicide include Dianat, Banvel, Diablo, Oracle and Vanquish. This chemical compound is a chlorinated derivative of o-anisic acid. [5]

  7. Methyl anisate - Wikipedia

    en.wikipedia.org/wiki/Methyl_anisate

    Methyl anisate is the methyl ester of p-anisic acid. It is found in star anise. It is an organic compound commonly used within the food industry. It is also commonly employed as a fragrance for certain perfumes. This compound can be synthesized directly through the condensation of methanol and 4-methoxybenzoic acid.

  8. Pinnick oxidation - Wikipedia

    en.wikipedia.org/wiki/Pinnick_Oxidation

    clo 2 − + h 2 po 4 − ⇌ hclo 2 + hpo 4 2− First, the chlorous acid adds to the aldehyde. Then resulting structure undergoes a pericyclic fragmentation in which the aldehyde hydrogen is transferred to an oxygen on the chlorine, with the chlorine group released as hypochlorous acid (HOCl).

  9. 2-Methoxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/2-methoxybenzaldehyde

    2-Methoxybenzaldehyde is an organic compound with the formula CH 3 OC 6 H 4 CHO. It is also commonly referred to as o-anisaldehyde. As a methylated version of salicylaldehyde, the molecule consists of a benzene ring with adjacent formyl and a methoxy groups. It is a colorless solid with a pleasant aroma.