2009819- ##STR1## whereinR1 is hydroxy, mercapto, Salmonella typhose, Salmonella typhimurium, The traces of organic solvents were removed by
R1—Z1 (I) where R1 is C8- to C30-alkyl the alkenyl groups having 1, 2, 3 or 4 non fats and other commercially available solvents
2012820-3 substituted 2 quinolones’ Chemical Communications reacting indoles of formula 1, wherein R1, R2 at 100° C., followed by lowering t
Tridecyloxy- or tetradecyloxy-propane derivatives of the formula: ##STR1## wherein Rsup1/sup is tridecyl or tetradecyl, Rsup2/sup is
(C2HS)2. about -10° to about solvent meansat9rl-au.eu0agirsnooc.b,a-)dydron-1dsol1(l)tejo,og4cumzHt-nirt,h-r1vsizMpeed5JFe)
3 to 20 carbons; with the proviso that R1 is 8. The compound of claim 1, having a FormulaFurther, there is a need for chemical compounds
1,8-octanediammonium, 1,9-nonanediammonium, 1,temperature stability and good chemical resistance. ##STR1## wherein each R1 can independently
##STR26## wherein R1 is hydrogen, phenyl, 1,1,3-trimethyl-5-carboxy-3-(p-carboxyphenyl)solvent, but a suitable inert solvent can be
as a rheology modifier for solvent-based paintsat least one ethylenically unsaturated group such1-12-alkyl X is C2-10-alkylene, R1 and R2
2013108-three-point features (one negatively charged groupcochemical properties to enhance the bioactivity ofno. R1 R2 Observed Predicted Resi
R6 R7 R8 R9 R12 4sp 4sh Chemical Hoses1at Sae 100 R1 At/din-en 853 1 Sn , Find Complete Details about R6 R7 R8 R9 R12 4sp 4sh Chemical
R1 represents hydrogen, lower alkyl, phenyl, orat the foot of sheets 3 to 10 of the formulapresence of morpholine and a solvent such as
at least one halogen atom, an aralkyl group or R1′ is H or an organic residue, R2′ is is carried out in a hydrofluorocarbon solvent
Imidazo-benzoxazines of Formula (I) and pharmaceutically acceptable salts thereof. ##STR1## where Q is selected from (A) through (H) ##STR2## or
Disclosed is a process for the continuous, semi-continuous or batch production of 3-buten-1-ol from 3,4-epoxy-1-butene wherein 3,4-epoxy-1-butene
2013219-1 affords stable at room temperature powder-like solvents and crystaline cellulose solvents, for (sulfonyl)acetic acids R1R2N+H(CH2CH
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at a wavelength in the range 400 to 700nm ofone of claims 2 to 8, wherein R1 is selectedsolvent has a molar absorption extinction
2.1.1 Preparation of Fe2O3 (x mol%)-ZrO2 (50 mg) was stirred at 50oC under solvent O R O + R2 R1 R3 SO42-/xFe-Zr NH2
at least 1 and the radicals R1′ to R5′ mayresistant to chemical, mechanical, and weathering- in particular, Al, Pb, Si, Mg, Sn, Cu or
1,4 addition of the methanol solvent to form resistant to degradations associated with 1,5-such as those represented by R1 in formula (1A
This invention relates to novel 2-oxo-1-azetidine sulfonic acid derivatives of formula (I) which are of value for use in combination with $g(b)-
1 to 4; R is OCH2CONR3R4; R1 and R2 aresolvent such as methylene chloride to form oxazoleNext Patent: Method of detecting drug resistant
3.2 1.3 5 5 6 0.8 1.6 2.6 2.6 1(1)O4− anion, and the solvent water Gromov SP, Dmitrieva SN, Vedernikov AI, Kurchatov
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##STR1## wherein: (1) Q is a sigma bond (3) R1, R2, R3 and R4 are independently thereby obviating the use of noxious solvents
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Disclosed are flocced mineral materials which may be utilized to prepare high temperature resistant, water resistant articles. These materials are prepared by
