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  2. Benzophenone imine - Wikipedia

    en.wikipedia.org/wiki/Benzophenone_imine

    Primary amines can be protected as benzophenone imines, and the protected amines are stable in flash chromatography. [7] Buchwald-Hartwig amination involves coupling aromatic halide and amine to form carbon-nitrogen bonds with the help of palladium-based catalysts. Benzophenone imine can be used as an ammonia-equivalent in such reactions. [1]

  3. Benzophenone - Wikipedia

    en.wikipedia.org/wiki/Benzophenone

    Benzophenone is a naturally occurring organic compound with the formula (C 6 H 5) 2 CO, generally abbreviated Ph 2 CO. Benzophenone has been found in some fungi, fruits and plants, including grapes. [4] It is a white solid with a low melting point and rose-like odor [5] that is soluble in organic solvents. Benzophenone is the simplest ...

  4. Imine - Wikipedia

    en.wikipedia.org/wiki/Imine

    When R = H, the compound is a primary imine, when R is hydrocarbyl, the compound is a secondary imine. If this group is not a hydrogen atom, then the compound can sometimes be referred to as a Schiff base. [9] When R 3 is OH, the imine is called an oxime, and when R 3 is NH 2 the imine is called a hydrazone.

  5. C13H11N - Wikipedia

    en.wikipedia.org/wiki/C13H11N

    Benzophenone imine, an organic compound with the formula of (C 6 H 5) 2 C=NH 2-Aminofluorene , a synthetic arylamine Index of chemical compounds with the same molecular formula

  6. Amine value - Wikipedia

    en.wikipedia.org/wiki/Amine_value

    The amine value is useful in helping determine the correct stoichiometry of a two component amine cure epoxy resin system. [6] [7] [8]It is the number of Nitrogens x 56.1 (Mwt of KOH) x 1000 (convert to milligrams) divided by molecular mass of the amine functional compound.

  7. Oxime - Wikipedia

    en.wikipedia.org/wiki/Oxime

    In organic chemistry, an oxime is an organic compound belonging to the imines, with the general formula RR’C=N−OH, where R is an organic side-chain and R' may be hydrogen, forming an aldoxime, or another organic group, forming a ketoxime.

  8. Polyimine - Wikipedia

    en.wikipedia.org/wiki/Polyimine

    Polyimines can be synthesised via a condensation reaction between aldehydes and (primary) amines. [2] During this reaction, water is also formed as byproduct. Often, the synthesis can be performed at room temperature, but to fully cure the materials and remove remaining water, they can be dried at slightly elevated temperatures and/or in vacuum.

  9. Oxybenzone - Wikipedia

    en.wikipedia.org/wiki/Oxybenzone

    Oxybenzone or benzophenone-3 or BP-3 (trade names Milestab 9, Eusolex 4360, Escalol 567, KAHSCREEN BZ-3) is an organic compound belonging to the class of aromatic ketones known as benzophenones. It takes the form of pale-yellow crystals that are readily soluble in most organic solvents.