1.6- Dimethyl-4-isopropyl-naphthalene

The above example clearly points to nonenzymatic hydrolysis of 3,4-dimethyl-5-phenyloxazolidine (11.106). However, enzymatic hydrolysis cannot entirely be ruled out. A related compound, 3-isopropyl-5- [(naphthalen-... 

Decahydrocyclododecaoxazole. See Decahydrocyclododecaoxazole [1S-(1-a,4-a,4a-a,6-a,8-ap]-Decahydro-1,6-dimethyl-4-(1-methylethyl) naphthalene, didehydro deriv.. See Cadinene Decahydro-4-a-hydroxy-2,8,8-trimethyl-2-naphthoic acid, y-lactone. See Decahydro-2,8,8-trimethylnaphthalene-2,4a-carbolactone 1,2,3,3a,3bp,4,5,6,6ap,6ba-Decahydro-1a-isopropyl-3aa-methyl-6-methylene-cyclobuta [1,2 3,4] dicyclopentene. See p-Bourbonene Decahydronaphthalene CAS 91-17-8 EINECS/ELINCS 202-046-9 UN 1147 (DOT)... 

Benzene, toluene, the xylenes, ethyl benzene, styrene, isopropyl benzene (cumene), chlorobenzene, the dichlorobenzenes, nitrobenzene, diphenyl, naphthalene, 1-methyl-naphthalene, 2-methyl-naphthalene, 2,6-dimethyl-naphthalene, and 2,6-diisopropyl naphthalene are the most important volatile aromatics of commercial significance. These compounds do not occur in the environment naturally except as constituents of petroleum which may seep into the oceans from underground deposits. The occurrence of these products in the environment is thus mainly or exclusively of man-made origin, as distinct from other hydrocarbons such as methane, terpenoids, polycyclic aromatics. 

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