Results 171 to 180 of about 12,121 (212)

Nonclassical oxidation of cymenes

Journal of the Chemical Society D: Chemical Communications, 1971
Cobalt(III) ion-catalysed co-oxidation of p-cymene and butane affords predominantly p-isopropylbenzoic acid, contrary to the prediction based on the classical free-radical mechanism.
Anatoli Onopchenko   +2 more
openaire   +1 more source

Health beneficial and pharmacological properties of p-cymene

Food and Chemical Toxicology, 2021
p-cymene also known as p-cymol or p-isopropyltoluene is an alkyl-substituted aromatic compound naturally occurring in essential oils (EOs) of various aromatic plants, including the genus of Artemisia, Protium, Origanum, and Thymus. It is related to the family of terpenes, especially monocyclic monoterpenes.
Abdelaali Balahbib   +9 more
openaire   +2 more sources

8-amino-p-cymene from p-cymene-trichloramine-aluminum chloride-t-butyl halide

Tetrahedron, 1967
Abstract p-Cymene was aminated on the isopropyl side-chain with trichloramine-aluminum chloride-t-butyl halide. At optimum conditions (p-cymene:trichloramine:aluminum chloride:t-butyl bromide = 1:0·1:0·2:0·3: 0–10°), 8-amino-p-cymene was obtained in 80% yield. Changes in temperature resulted in slightly lower yields.
P. Kovacic, R.J. Hooper
openaire   +1 more source

[RuCl2(PH2Cy)(η6-p-cymene)]

Acta Crystallographica Section C Crystal Structure Communications, 1994
The structure of dichloro(cyclohexylphosphine)(η 6 -p-cymene)ruthenium, [RuCl 2 (η 6 -C 10 H 14 )(C 6 H 13 P)], is reported. The structure determination shows that the C atoms of the aromatic six-membered ring are almost equidistant from the Ru atom, at distances close to the average value of 2.21 (3) A. The other metal-ligand distances are Ru-P 2.299 (
J. F. Van der Maelen Uría   +3 more
openaire   +1 more source

ChemInform Abstract: NITRATION OF P‐CYMENE. EXCHANGE AND REAROMATIZATION REACTIONS OF P‐CYMENE ADDUCTS

Chemischer Informationsdienst, 1976
AbstractNitrierung von p‐Cymol (I) in Acetanhydrid liefert ein Gemisch der cisund trans‐Nitroacetate (II) (Hauptprodukt), die Nitrocymole (III) und das Nitrotoluol (IV).
ALFRED FISCHER, ROLF ROEDERER
openaire   +1 more source

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