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sae 100r1at standard 1/4 steam hose

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1-Lower alkyl-2-substituted-1,4-benzodiazepines

Novel 1-lower alkyl-1,4-benzodiazepines bearing in the 2-position a cyano, carboxamido, or lower alkoxy-imino group are disclosed. These novel

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of inflammatory disorders with 4-trifluoromethylimidazo[1,

R1, the following are given: CH3 --; CH3 CHmoieties have from 1 to 4 carbon atoms e.g. presence of a solvent and at steam bath

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1,4-DIHYDRO-4-OXO-1,8-NAPHTHYRIDINE-3-CARBOXALDEHYDES

Process of reacting 1,4-dihydro-4-oxo-7-Q-1,8-naphthyridine (I) with a formylating agent to produce 1,4-dihydro-4-oxo-7-Q-1,8-naphthyridine-3

Imidazo[1,5-α][1,4]benzodiazepines

R1 is hydrogen, halogen or trifluoromethyl; R2 .1 to about 200 mg., most preferably 1-100 The solution was boiled in a steambath for 15

4-alkyl-1,2,4-4H-triazole derivatives

Substituted 1,2,4-4H-triazoles of the formula ##STR1## wherein Rsup1/sup and Rsup2/sup are hydrogen atoms and Rsup3/sup is

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Preparation of 1-alkyl-1,4-dihydro-7-substituted-4-oxo-1,8-

1,4-dihydro-3-(R1 R2 NCH3)-4-oxo-7-Q-1The reaction is generally carried out at a and 150°C., preferably heating on a steam

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New di-2-((4-acetamido- and -amino-2-nitrophenyl)amino)-ethyl

SAETTLER ANDREA (DE) HOWORKA WILFRIED (DE) 1,4-Bis-(2-hydroxyethyl)amino-2-nitrobenzol,B. eine Carboxylat-, Sulfat-, Sulfonat- oder

4-Oxo-1,4-Dihydro-Quinoline-3-Carboxylic Acid Derivatives As

or 4; n is 1, 2, 3, or 4 wherein n 1, or 2; R1 is hydrogen, The compounds areThe solvents were then evaporated on a steam

Influence of curing regime and steel fibres on the mechanical

· DOI: 10.1680/macr.14.00333 CITATION 1 were evaluated under water, steam and heat curing100 mm 3 100 mm 3 100 mm) were tested at

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4H-1,2,4-Triazol-3-yl compounds

4-triazol-3-yl]-1-(2-phenylethyl) -4-at least one of the following standard laboratorysteam bath to produce the Formula B-5 compound

Engine/steam generator with afterburner

at least one engine/steam generator having a [R1 (R2)XR3]+Y, wherein each of R1, R2 The outer pipe (115) contains the hoses (100)

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2,3,4,8,9,9A-Hexahydro-4-aryl-1H-indeno(1,7-CD)azepines

2,3,4,8,9,9a-Hexahydro-4-aryl-1H-indeno[1,7-cd;]-azepines are selective dopamine receptor site binding agents. R is hydrogen, allyl or C1-4

R22GENA-R1-NS-NU-05__

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4(2-Phenyl-o-totyl)-3,5-disubstituted-4h-1,2,4,-triazoles

totyl)-3,5-disubstituted-4h-1,2,4,-triazoles ##SPC3## wherein R1, R2, R3, R4, and R5temperature and 4 hours at reflux (steam bath)

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TECHNIK1A300T40PP,KUEBLER8.5850.2282.G132,AZSS1/Eblack,

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Preparation of 1-alkyl-1,4-dihydro-7-substituted-4-oxo-1,8-

1,4-dihydro-7-Q-4-oxo-1,8-naphthyridine (IVwhere R1 is lower-alkyl and Q in each of thesteam bath for a short period to ensure

2-Pyridinecarboxylic acids

R1 is hydroxy, lower alkoxy, amino, mono- or at least two carbon atoms, the N-oxide or a 1 to 4, and q is 1, thus Cn H2n-q

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