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Ethyl 2- -, ethy

When a-positions in thienothiophenes 1 and 2 are both blocked, the formyl group enters a /7-position. Thus, formylation of 5-ethyl-2-ethy lthiothieno [2,3-6] thiophene and 5-ethyl-2-ethylthiothieno[3,2-h]-thiophene afforded high yields of the 3-formyl derivatives220 [Eqs. (64) and (65)]. 2-Ethylthiobenzo[h]thiophene reacts analogously. [Pg.191]

Rhodacyanines possess two chromophoric systems. They are at the same time neutrocyanine derivatives, which involves position 5 of the ketomethylene, and methine cyanine, which involves position 2. Following lUPAC s standard nomenclature rules, structure 7 is named 3-ethyl-4-phenyl-2- 4-oxo-3-ethyl-5-[2-(3-ethy]-2,3-dihydro-benzo-l,3-thiazo-lylidene)ethylidene]-tetrahydro-l,3-thiazolylidene-methyl -1.3-thiazolium iodide (Scheme 5). It implies that the 4-phenyl thiazole ring having the... [Pg.27]

Chemical Name [ (3-(2-(Diethylamino)ethy ] -4-methyl-2-oxo-2H-1 -benzopyran-7-yl] oxy) acetic acid ethyl ester hydrochloride... [Pg.336]

Ethy I-2-(3-hydroxy-4-ami nophenyl) propio nate Benoxaprofen Ethyl p-hydroxybenzoate Cyclomethycaine... [Pg.1634]

N-Ethy I-N-2-hydroxy ethylamine Hydroxychloroquine sulfate Ethyl a-hydroxyisobutyrate Trimethadione Ethyl iodide... [Pg.1634]

Note TLC was performed on silica gel, and the solvents were (1) -bntanol/glacial acetic acid/water (2 1 1, v/v), (IV) isoamyl alcohol/ethy methyl ketone/glacial acetic acid/water (40 40 7 13, v/v), (VII) n-bntanol/2-propanol/water/glacial acetic acid (30 50 10 2, v/v), (VIII) ethyl methyl ketone/acetic acid/methanol (3 1 1, v/v), and (IX) n-bntanol/benzyl alcohol/glacial acetic acid (8 4 3, v/v). [Pg.239]

Ethy Ibenzy lamine A -Methyl o-toluidine A -Methyl m-toluidine. 2V-Methyl p-toluidine A -Ethyl o-toluidine -Ethyl m-toluidine -Ethyl p-toluidine 2V-Methyl a-naphthylamine 2V-Methyl p-naphthylamine 2V-Phenyl- a-naphthylamine N-Phenyl- p-naphthylamine... [Pg.659]

Methyl-l//-pyrimido[l,2-rz]quinolin-l-one was obtained by heating isopropylidene 2-[l-(2-quinolylamino)ethy-lidene]malonate in EtOH at 20 °C <2000CCL283>. FVT of ethyl 3-morpholino- and 3-(Ar-methyl-Ar-phenylamino)-... [Pg.185]

Disulfuryl dilluoride, 4326 f Ethyl chloroformate, 1164 Ethyl oxalyl chloride, 1456 /V-Ethy l-/V-propylcarbamoyl chloride, 2468... [Pg.27]

Siehe ferner die Arbeitsvorsehrift zur Herstellung von Bis-[nitro-(2,2,2-trinitro-ethyl)-amino -furazan-2-oxid (65%) aus l-Diazo-3-[nitro-(2,2,2-trinitro-ethy])-amino]-2-oxo-propan in Bd. IV/la, S. 806. [Pg.739]

Als Base dient hierbei ein doppelter OberschuB an Amin. Die Produkte (z.B. Bis-[l,l-diethyl-propinyl]-amitv, 48%) konnen, je nach Bedingungen, zu sterisch stark gehinderten primaren Aminen (z. B. H2/Pt02/Ethanol, 300 kPa 3-Amino-3-ethy -pentan 90%), sekundaren Aminen (z.B. H2/Raney-Ni/Ethanol, 420kPa Bis-[1, l-diethyl-propyl]-amin 72%) Oder cyclischen Aminen (z.B. Hj/Pd-C/Ethanol, Normaldruck, 0° 2,2,5,5-Tetra-ethyl-3,4-dimethyl-2,5-dihydro-pyrrol, 48% neben 2,2,5,5-Tetraethy -4-methyl-3-methylen-pyrrolidin 15%) hydriert werden. [Pg.666]

N-Ethyl-(dimethylphenyl)- amine or N-Ethy -dimethylaniline and Derivatives (Xthyl-vic-o-xylidin in Ger),... [Pg.99]

Similarly, with acetaldehyde and propionaldehyde as the starting materials, one gets the 2,4-dimethyl-6-ethyl- and 2-ethy 1-4,6-dimethyl derivatives (33,37), In the presence of acetaldehyde, the higher aldehydes give various substituted... [Pg.43]

MP 30, 103-06(1948) 8c CA 44, 7242(1950) N,N -Dinitro-N,Nl-di(2 -nitroxyethyl)-oxamide N,N Dinitro-N,N-di 2-ethy lol)-oxamide Dinitrate N,N<-Dinitro-N,Nl -bis(2-hydroxy-ethyl)-oxainide Dinitrate (CA nomenclature) or Bis-(nitroxyethylnitro)-oxamide, abbreviated as NENO [called N.N -Dinitro-N.N bis (2-nitryloxy-athyl)-oxamid or Disalpeter-saureester des N.N -Dinitro-N.N -bis(2-hydroxy-athyl)-oxamids in Ger and Dinitrate du Dioxyethyldinitrooxamide in Fr],... [Pg.138]


See other pages where Ethyl 2- -, ethy is mentioned: [Pg.69]    [Pg.96]    [Pg.54]    [Pg.349]    [Pg.303]    [Pg.66]    [Pg.567]    [Pg.6]    [Pg.149]    [Pg.963]    [Pg.224]    [Pg.237]    [Pg.290]    [Pg.1018]    [Pg.600]    [Pg.81]    [Pg.81]    [Pg.167]    [Pg.186]    [Pg.406]    [Pg.252]    [Pg.237]   


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1-Ethy 1-3-

Ethyl 2- -, ethy ester

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