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L-methyl-2-isopropylbenzene

Chloro-3-hydroxy-l-methyl-4-isopropylbenzene 6-diazonium chloride 3 C258... [Pg.518]

Chloro-3-hydroxy-l-methyl 4-isopropyl-benzene -6-diazoniumchloride, HO.CgH.CI(CH3) [CH -(CH3)2], N(iN).Cl mw 24 9.12, N 10.99% col ndls (from eth-alc), mp explodes on heating was prepd by treating a cold ale soln of 2-chloro-6 -amino-3-hydroxy-l-methyl-4-isopropylbenzene with nitrous acid(Refs 1 2)... [Pg.41]

Addo trimico 3-p-cymenol p-cymen-3-ol Flavinol 3-hydroxy-p-cymene 3-hydroxy-l-methyl-4-isopropylbenzene Intrasol isopropyl cresol isopropyl-w-cresol 6-isopropyl-m-cresol isopropyl metacresol 2-isopropyl-5-methylphenol 1-methyl-3-hydroxy-4-isopropylbenzene 5-methyl-2-isopropyl-phenol 5-methyl-2-(l-methylethyl) phenol Medophyll thyme camphor thymic acid m-thymol timol. [Pg.780]

The sulfonation of p-cymene (l-methyl-4-isopropylbenzene) gives the 2-sulfonic acid. Is this the expected orientation Explain. Use this fact to synthesize carvacrol, 2-methyl-5-isopropylphenol, from p-cymene. Carvacrol is found in the essential oils from thyme, marjoram, and summer savory. It has a pleasant thymol-like odor. [Pg.1280]


See other pages where L-methyl-2-isopropylbenzene is mentioned: [Pg.291]    [Pg.409]    [Pg.511]    [Pg.566]    [Pg.602]    [Pg.516]    [Pg.727]    [Pg.871]    [Pg.53]    [Pg.2217]    [Pg.2380]    [Pg.308]    [Pg.500]    [Pg.96]    [Pg.96]    [Pg.96]    [Pg.96]    [Pg.96]    [Pg.96]    [Pg.96]    [Pg.96]    [Pg.2346]    [Pg.2430]    [Pg.27]   
See also in sourсe #XX -- [ Pg.75 ]




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1- Methyl-4-isopropylbenzene

Isopropylbenzene

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