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Methyl benzoate is an organic compound. It is an ester with the chemical formula C 6 H 5 COOCH 3 , sometimes abbreviated as PhCO 2 Me , where Ph and Me are phenyl and methyl , respectively. Its structure is C 6 H 5 −C(=O)−O−CH 3 .
a (L 2 bar/mol 2) b (L/mol) Acetic acid: 17.7098 0.1065 Acetic anhydride: 20.158 0.1263 Acetone: 16.02 0.1124 Acetonitrile: 17.81 0.1168 Acetylene: 4.516 0.0522 Ammonia: 4.225 0.0371 Aniline [2] 29.14 0.1486 Argon: 1.355 0.03201 Benzene: 18.24 0.1193 Bromobenzene: 28.94 0.1539 Butane: 14.66 0.1226 1-Butanol [2] 20.94 0.1326 2-Butanone [2] 19.97 ...
Density: 1.2659 g/cm 3 ... Solubility in water. 1.7 g/L ... are obtained by transesterification of methyl benzoate with the corresponding diol. ...
Substance Formula 0 °C 10 °C 20 °C 30 °C 40 °C 50 °C 60 °C 70 °C 80 °C 90 °C 100 °C Barium acetate: Ba(C 2 H 3 O 2) 2: 58.8: 62: 72: 75: 78.5: 77: 75
Methyl tert-butyl ether (MTBE), also known as tert-butyl methyl ether, is an organic compound with a structural formula (CH 3) 3 COCH 3. MTBE is a volatile, flammable, and colorless liquid that is sparingly soluble in water. [ 1 ]
Liquid water has a density of approximately 1 g/cm 3 (1 g/mL). Thus 100 mL of water is equal to approximately 100 g. Thus 100 mL of water is equal to approximately 100 g. Therefore, a solution with 1 g of solute dissolved in final volume of 100 mL aqueous solution may also be considered 1% m/m (1 g solute in 99 g water).
One method involves its conversion to the Grignard reagent, phenylmagnesium bromide. This reagent can be used, e.g. in the reaction with carbon dioxide to prepare benzoic acid. [4] Other methods involve palladium-catalyzed coupling reactions, such as the Suzuki reaction. Bromobenzene is used as a precursor in the manufacture of phencyclidine.
Benzylamine, also known as phenylmethylamine, is an organic chemical compound with the condensed structural formula C 6 H 5 CH 2 NH 2 (sometimes abbreviated as PhCH 2 NH 2 or BnNH 2).It consists of a benzyl group, C 6 H 5 CH 2, attached to an amine functional group, NH 2.