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  2. Propionaldehyde - Wikipedia

    en.wikipedia.org/wiki/Propionaldehyde

    Propionaldehyde exhibits the reactions characteristic of alkyl aldehydes, e.g. hydrogenation, aldol condensations, oxidations, etc. It is the simplest aldehyde with a prochiral methylene such that α-functionalized derivatives (CH 3 CH(X)CHO) are chiral. If water is available, propionaldehyde exists in equilibrium with 1,1-propanediol, a ...

  3. 1-Propanol - Wikipedia

    en.wikipedia.org/wiki/1-Propanol

    1-Propanol (also propan-1-ol, propanol, n-propyl alcohol) is a primary alcohol with the formula CH 3 CH 2 CH 2 OH and sometimes represented as PrOH or n-PrOH.It is a colourless liquid and an isomer of 2-propanol. 1-Propanol is used as a solvent in the pharmaceutical industry, mainly for resins and cellulose esters, and, sometimes, as a disinfecting agent.

  4. Isobutanol - Wikipedia

    en.wikipedia.org/wiki/Isobutanol

    Isobutanol (IUPAC nomenclature: 2-methylpropan-1-ol) is an organic compound with the formula (CH 3) 2 CHCH 2 OH (sometimes represented as i-BuOH). This colorless, flammable liquid with a characteristic smell is mainly used as a solvent either directly or as its esters.

  5. 2-Phenyl-2-propanol - Wikipedia

    en.wikipedia.org/wiki/2-Phenyl-2-propanol

    2-Phenyl-2-propanol can either be applied in organic syntheses, or be reactants or intermediates in agrochemical, medical, and dyestuff fields. [ 2 ] 2-Phenyl-2-propanol is the main metabolite of cumene , and therefore 2-phenyl-2-propanol can serve as a biomarker of cumene.

  6. 3-Methyl-3-pentanol - Wikipedia

    en.wikipedia.org/wiki/3-Methyl-3-pentanol

    3-Methyl-3-pentanol (IUPAC name: 3-methylpentan-3-ol) is an organic chemical compound and a tertiary hexanol. It is used in the synthesis of the tranquilizer emylcamate , [ 2 ] and has similar sedative and anticonvulsant actions itself.

  7. Propiophenone - Wikipedia

    en.wikipedia.org/wiki/Propiophenone

    It is also prepared commercially by ketonization of benzoic acid and propionic acid over calcium acetate and alumina at 450–550 °C: [1] C 6 H 5 CO 2 H + CH 3 CH 2 CO 2 H → C 6 H 5 C(O)CH 2 CH 3 + CO 2 + H 2 O. Ludwig Claisen discovered that α-methoxystyrene forms this compound when heated for an hour at 300 °C (65% yield). [2] [3]

  8. Phenylpropanoic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylpropanoic_acid

    Density: 1.126 g/cm 3: Melting point: 47 to 50 °C (117 to 122 °F; 320 to 323 K) Boiling point: 280 °C (536 °F; 553 K) Solubility in water. 5.9 g/L log P:

  9. Propylamine - Wikipedia

    en.wikipedia.org/wiki/Propylamine

    C 3 H 9 N: Molar mass: 59.112 g·mol −1 Appearance Colorless liquid Odor: fishy, ammoniacal Density: 0.719 g mL1: Melting point: −83.00 °C; −117.40 °F; 190.15 K Boiling point: 47 to 51 °C; 116 to 124 °F; 320 to 324 K