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Butan-2-yl (sec-butyl) group is chiral. The carbon atom at position 2 is a stereocenter. It has four different groups attached: −H, −CH 3, −CH 2 −CH 3, and −R (the R group is not equal to those three groups). The names of the two chiral groups are: (2S)-butan-2-yl and (2R)-butan-2-yl.
(Butan-2-yl)benzene. Other names sec-butylbenzene; ... Its structure consists of a benzene ring substituted with a sec-butyl group. It is a flammable colorless liquid ...
The product of this reaction is 2-(1-methylpropyl)phenol. The second step in the synthesis of dinoseb is the nitration of 2-(1-methylpropyl)phenol. First, the nitronium ion is formed from nitric acid and sulfuric acid. [21] 2-(1-methylpropyl)phenol takes up the nitronium ion to form the arenium ion, which has three resonance structures. Water ...
sec-Butylamine is an organic chemical compound (specifically, an amine) with the formula CH 3 CH 2 CH(NH 2)CH 3. It is a colorless liquid. sec-Butylamine is one of the four isomeric amines of butane, the others being n-butylamine, tert-butylamine, and isobutylamine. sec-Butylamine is chiral and therefore can exist in either of two enantiomeric ...
sec-Butyl acetate, or s-butyl acetate, is an ester commonly used as a solvent in lacquers and enamels, where it is used in the production of acyclic polymers, vinyl resins, and nitrocellulose. [3]
Binapacryl was used as a miticide and fungicide.Chemically, it is an ester derivative of dinoseb.Although binapacryl has low toxicity itself, it is readily metabolized to form dinoseb, which is highly toxic.
Butralin's major soil metabolite is 4-tert-butyl-2,6-dinitroaniline. [15] Other major metabolites see the loss of more or all of the carbons and hydrogen over the nitrogen, or loss of oxygen from the nitro groups.
2-(Butan-2-yl)phenol. Other names 2-(1-Methylpropyl)phenol ... 16 °C; 61 °F; 289 K [2] Boiling point: 230 °C (446 °F; 503 K) [1] Vapor pressure: 4.74 Pa (25 °C) [1]