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  2. 4-Carboxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-Carboxybenzaldehyde

    4-Carboxybenzaldehyde (CBA) is an organic compound with the formula OCHC 6 H 4 CO 2 H. It consists of a benzene ring substituted with both an aldehyde and a carboxylic acid, with these functional groups on opposite corners of the ring. This compound is formed in 0.5% yield as a byproduct in the production terephthalic acid from p-xylene. Since ...

  3. Benzoic acid - Wikipedia

    en.wikipedia.org/wiki/Benzoic_acid

    The name is derived from gum benzoin, which was for a long time its only source. Benzoic acid occurs naturally in many plants [9] and serves as an intermediate in the biosynthesis of many secondary metabolites. Salts of benzoic acid are used as food preservatives. Benzoic acid is an important precursor for the industrial synthesis of many other ...

  4. IUPAC nomenclature of chemistry - Wikipedia

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

    IUPAC states that, "As one of its major activities, IUPAC develops Recommendations to establish unambiguous, uniform, and consistent nomenclature and terminology for specific scientific fields, usually presented as: glossaries of terms for specific chemical disciplines; definitions of terms relating to a group of properties; nomenclature of chemical compounds and their classes; terminology ...

  5. 4-Formylphenylboronic acid - Wikipedia

    en.wikipedia.org/wiki/4-Formylphenylboronic_acid

    4-Formylphenyl boronic acid crystallizes in colorless needles [1] or is obtained as an odorless, whitish powder, which dissolves little in cold but better in hot water. The compound is quite stable [3] and readily forms dimers and cyclic trimeric anhydrides, which complicate purification and tend to protodeboronize, a secondary reaction that occurs frequently in the Suzuki coupling, with ...

  6. Quinisocaine - Wikipedia

    en.wikipedia.org/wiki/Quinisocaine

    Thieme Synthesis: [2] [3] Patent: [4] [5] The Henry reaction between phthalaldehydic acid (2-Formylbenzoic acid) [119-67-5] (1) and 1-nitropentane [628-05-7] occurs by a mechanism that involves a hydroxy acid (2). Expulsion of water then gives (3). Reduction of the nitro group via catalytic hydrogenation leads to the amine, CID:158569430 (4).

  7. 4- (4-Chlorophenoxy)butanoic acid - Wikipedia

    en.wikipedia.org/wiki/4-(4-chlorophenoxy...

    4-(4-Chlorophenoxy)butanoic acid is an herbicide. Its formula is C 10 H 11 ClO 3 . It is an approved substance under the name 4-CPB by the Weed Science Society of America .

  8. 4-Mercaptobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/4-Mercaptobenzoic_acid

    4-Mercaptobenzoic acid (p-mercaptobenzoic acid, p-MBA) is an organosulfur compound with the formula para-C 6 H 4 (−SH)(−COOH). It is used as a ligand in thiolate-protected gold cluster compounds, such as Au 102 ( p -MBA) 44 .

  9. 2-Carboxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/2-Carboxybenzaldehyde

    The reaction of bromine with phthalide produces 2-bromophthalide, which is converted into 2-formylbenzoic acid by heating with water in a total yield of 78 to 83%. [4] Synthese von 2-Carboxybenzaldehyd aus Phthalid. An analogous process based on a chlorination reaction can also be used: [5]