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  2. Boronic acid - Wikipedia

    en.wikipedia.org/wiki/Boronic_acid

    The general structure of a boronic acid, where R is a substituent.. A boronic acid is an organic compound related to boric acid (B(OH) 3) in which one of the three hydroxyl groups (−OH) is replaced by an alkyl or aryl group (represented by R in the general formula R−B(OH) 2). [1]

  3. Borinic acid - Wikipedia

    en.wikipedia.org/wiki/Borinic_acid

    Borinic acid, also known as boronous acid, is an oxyacid of boron with formula H 2 BOH. Borinate is the associated anion of borinic acid with formula H 2 BO −; however, being a Lewis acid, the form in basic solution is H 2 B(OH) − 2. Borinic acid can be formed as the first step in the hydrolysis of diborane: [1] BH 3 + H 2 O → H 2 BOH + H 2

  4. Phenylboronic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylboronic_acid

    Phenylboronic acid or benzeneboronic acid, abbreviated as PhB(OH) 2 where Ph is the phenyl group C 6 H 5 - and B(OH) 2 is a boronic acid containing a phenyl substituent and two hydroxyl groups attached to boron. Phenylboronic acid is a white powder and is commonly used in organic synthesis.

  5. Phthalaldehyde - Wikipedia

    en.wikipedia.org/wiki/Phthalaldehyde

    Phthalaldehyde (sometimes also o-phthalaldehyde or ortho-phthalaldehyde, OPA) is the chemical compound with the formula C 6 H 4 (CHO) 2. It is one of three isomers of benzene dicarbaldehyde, related to phthalic acid. This pale yellow solid is a building block in the synthesis of heterocyclic compounds and a reagent in the analysis of amino ...

  6. Monobromophenol - Wikipedia

    en.wikipedia.org/wiki/Monobromophenol

    Boiling point: 195–196 °C [1] 236 °C [2] 235–236 °C [3] pKa [4] 8.42: 9.11: 9.34 GHS hazard pictograms [1] [2] [3] GHS hazard statements: H226, H302, H315 ...

  7. Lithium borohydride - Wikipedia

    en.wikipedia.org/wiki/Lithium_borohydride

    Lithium borohydride (LiBH 4) is a borohydride and known in organic synthesis as a reducing agent for esters.Although less common than the related sodium borohydride, the lithium salt offers some advantages, being a stronger reducing agent and highly soluble in ethers, whilst remaining safer to handle than lithium aluminium hydride.

  8. Triethylammonium acetate - Wikipedia

    en.wikipedia.org/wiki/Triethylammonium_acetate

    Boiling point: 164.5 °C (328.1 °F; 437.6 K) ... [4] Since unadjusted triethylammonium acetate salt solutions contain neither a conjugate acid nor a conjugate base, ...

  9. Vinyl neodecanoate - Wikipedia

    en.wikipedia.org/wiki/Vinyl_neodecanoate

    Vinyl neodecanoate (trade name VeoVa 10) is a vinylic monomer that is virtually always used in combination with other monomers to create latices or emulsion polymers. [3] The trade name is an acronym of Vinyl ester of Versatic Acid with the number 10 meaning 10 carbons in the molecule.