2-Ethoxy-2-methylpropan

Chloroethane, Chloroform, Diethyl phthalate. Ethyl acetate. Ethyl acrylate. Ethyl bromide. Ethyl ether. Ethyl formate. Formaldehyde, Methoxychlor, Nitromethane, Parathion, Phorate. Ouizalofop-ethvl Ethanolamine, see Ethylenimine, Morpholine Ethoxyacetaldehyde, see 2-Ethoxyethanol 2-Ethoxy-2-methylpropanal, see Ethyl tert-butvl ether Ethylacetamide, see Dimethylamine, Triethylamine Ethyl acetate, see Nitromethane, Tetrachloroethylene... 

CASRN 637-92-3 molecular formula CeH O FW 102.17 Chemical/Physical The atmospheric oxidation of ethyl ferf-butyl ether by OH radicals in the presence of nitric oxide yielded ferf-butyl formate as the major product. Minor products included formaldehyde and nitrogen dioxide. In the absence of nitric oxide, 2-ethoxy-2-methylpropanal is likely to form (Wallington and Japar, 1991). 

Dr. Don T. Doit wanted to synthesize the anesthetic 2-ethoxy-2-methylpropane. He used ethoxide ion and 2-chloro-2-methyl-propane for his synthesis and ended up with very little ether. What was the predominant product of his synthesis What reagents should he have used ... 

Ethoxy-2-methylpropane see tert-Butyl ethyl ether... 

Kim, Y. Keskinen, K. L Aittamaa, J. Vapor-liquid equilibrium for binary systems 2-propanol + 2-ethoxy-2-methylpiopane and ethyl ethanoate + 2-ethoxy-2-methylpropane at 333 K and 2-propanone + 2-ethoxy-2-methylpropane at 323 K J. Chem. Eng. Dam 2004,49, 1273-1278... 

CsHmO 637-92-3 tert-Butyl ethyl ether syn. dETBE 2-Ethoxy-2-methylpropane... 

N-(2- [Ethoxy(methyl)phosphoryl]sulfanyl ethyl)-IV-isopropyl-N-methylpropan-2-aminium Iodide N-(2- [Ethoxy(methyl)phosphoryl]sulfanyl ethyl)-IV-isopropylpropan-2-aminium Chloride N-(2-Chloroethyl)dimethylamine N-(2-Chloroethyl)-N,N-dimethylamine N-(2-Hydroxyethyl)diethylamine N-(4-Oxy-3-methoxybenzyl)-8-methyl-6-nonenamide N-(Diethylamino)ethanol N-(Isopropyl)-2-propamine... 

Azetidin-2-one can be synthesized by treating 1-ethoxy-1-hydroxycy-clopropane with aqueous sodium azide at pH 5.5 (Scheme 8.7a). This type of construction has wider applications and A-substituted derivatives are formed from 1-amino-1-hydroxycyclopropanes in two steps first A-chlorination with tert- miy hypochlorite [2-methylpropan-2-yl chlo-rate(I)], and then treatment with silver ion in acetonitrile (ethanenitrile) to release chloride ion and trigger ring expansion of the tricycle (Scheme 8.7b). 

Depending on the reaction conditions used for hydrolysis, either 3-benzoyl-amino-5-methylpyran-2-one 489 or 3-methylpyrrole 492 have been obtained from the 3-ethoxy-2-methylpropanal derived unsaturated oxazolone 487 (Scheme 7.156). ... 

Methoxycyclohexene l-Ethoxy-2-methylpropane Allyl vinyl ether... 

Figure 12.17 Several multifunctional initiators used for making star (co)polymers. (VIII) 2-((2,2-bis(hydroxymethyl) butoxy) carbonyl)-2-methylpropane-l,3-diyl bis(2-bromo-2-methyl propanoate) (Yang etal.,2008). (IX) l,l,l-tris(4-(2-bromoisobutyryloxy) phenyl) ethane (Matyjaszewski etal., 1999). (X) 2-(hydroxymethyl)-2-methyl-3-oxo-3-(2-phenyl-2-(2,2,6,6-tetramethyl piperidin-l-yloxy)ethoxy) propyl pent-4-ynoate (Altintas et al., 2008). (XI) propargyl 2-hydroxylmethyl-2-(or-bromoisobutyryloxymethyl)propion-ate (Altintas et al., 2008).

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