Octenes 2-octene

Other allylic oxidation products are 2-octenal, 1 -octene-3-ol, l-octene-3-one, 2-octene-I-ol. 

Reaction of Carbon Tetrachloride with Octene-1 Octene-1 (b.p. 121.2°C (750 mm.) (37 g., 0.33 mole), carbon tetrachloride (154 g., 1.0 mole) and benzoyl peroxide (5 g., 0.02 mole) were heated together under an excess pressure of 15 cm. of mercury. Carbon dioxide was steadily evolved for about 4 h, during which time the boiling point of the reaction mixture rose from 90 to 105°C. The excess of carbon tetrachloride was then removed by distillation, and the residue was distilled in vacuo. The forerun contained a small amount of a white solid material. A fraction (72 g) boiling at 75-85°C (0.05 mm.) was collected and redistilled. The yield of redistilled product was 66 g. (75%) b.p. 78-79°C (0.1 mm.). This material was 1,1,1,3-tetrachlorononane. 

AI3-28403 Caprylene 1-Caprylene EINECS 203-893-7 HSDB 1084 Octene Octene-1 a-Octene 1-Octene Octylene 1-Octylene n-1-Octene NSC 8457. Intermediate for surfactants and specialty industrial chemicals. Liquid mp = -101.7° bp = 121.2°. 0 = 0.7149 insoluble in H2O. slightly soluble in CQ4, soluble in Et20. MezCO. CeHe, very soluble in CHCI3. Air Products Chemicals Inc. Chevron Ethicon Inc. Shell Sigma-Aldrich Fine Chem. Texaco. 

N-Octadecane Octahydro-4,7-methano-1 H-indenecarbaldehyde y-Octalactone n-Octanal Octanal dimethyl acetal Octanal ethyleneglycol cyclic acetal 2-Octanol 3-Octanol 3-Octanone 2-Octenal trans-2-Octenal 1-Octen-3-ol 1-Octen-3-yl acetate Octyl acetate 3-Octyl acetate Octyl butyrate Octyl formate Octyl isobutyrate Opopanax gum Orange (Citrus aurantium dulcis) peel wax Origanum oil 3-Oxabicyclo [10.3.0] pentadec-6-en Oxalide Palmarosa (Cymbopogon martini) oil Pennyroyal (Mentha pulegium) extract... 

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