Microbicidal active substances

The use of oxathiazolones of formula is described, R1 is C1-C16alkyl, C2-C16alkenyl or C5-C8cycloalkyl, each unsubstituted or substituted by halogen, -CN, -NO2, -C=O, -C=S, -NR2, -OR3, -SR4, -SO2R5, -COOR6 or by a 1,3,4-oxathiazol-2-one radical; C6-C10aryl unsubstituted or substituted by one or more...

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Main Authors SCHNYDER MARCEL, HOLZL WERNER
Format Patent
LanguageEnglish
Published 02.09.2004
Edition7
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Abstract The use of oxathiazolones of formula is described, R1 is C1-C16alkyl, C2-C16alkenyl or C5-C8cycloalkyl, each unsubstituted or substituted by halogen, -CN, -NO2, -C=O, -C=S, -NR2, -OR3, -SR4, -SO2R5, -COOR6 or by a 1,3,4-oxathiazol-2-one radical; C6-C10aryl unsubstituted or substituted by one or more C1-C5alkyl, C6-C10aryl, halogen, hydroxy, acyl, -CN, -CF3, -NO2, -NR2, -OR3, -SR4, -SO3H, -SO2R5, -COOR6 substituents or by a 1,3,4-oxathiazol-2-one radical; or a 5- or 6-membered heterocyclic radical; R2 and R3 are each independently of the other hydrogen; C1-C5alkyl; C6-C10aryl, or acyl; R4 is hydrogen; C1-C5alkyl; or C6-C10aryl; R5 is C1-C5alkyl; or C6-C10aryl; R6 is hydrogen; C1-C5alkyl; or C6-C10aryl, in the antimicrobial treatment of surfaces. The compounds exhibit a pronounced action against pathogenic gram-positive and gram-negative bacteria, and also against yeasts and moulds.
AbstractList The use of oxathiazolones of formula is described, R1 is C1-C16alkyl, C2-C16alkenyl or C5-C8cycloalkyl, each unsubstituted or substituted by halogen, -CN, -NO2, -C=O, -C=S, -NR2, -OR3, -SR4, -SO2R5, -COOR6 or by a 1,3,4-oxathiazol-2-one radical; C6-C10aryl unsubstituted or substituted by one or more C1-C5alkyl, C6-C10aryl, halogen, hydroxy, acyl, -CN, -CF3, -NO2, -NR2, -OR3, -SR4, -SO3H, -SO2R5, -COOR6 substituents or by a 1,3,4-oxathiazol-2-one radical; or a 5- or 6-membered heterocyclic radical; R2 and R3 are each independently of the other hydrogen; C1-C5alkyl; C6-C10aryl, or acyl; R4 is hydrogen; C1-C5alkyl; or C6-C10aryl; R5 is C1-C5alkyl; or C6-C10aryl; R6 is hydrogen; C1-C5alkyl; or C6-C10aryl, in the antimicrobial treatment of surfaces. The compounds exhibit a pronounced action against pathogenic gram-positive and gram-negative bacteria, and also against yeasts and moulds.
Author SCHNYDER MARCEL
HOLZL WERNER
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Snippet The use of oxathiazolones of formula is described, R1 is C1-C16alkyl, C2-C16alkenyl or C5-C8cycloalkyl, each unsubstituted or substituted by halogen, -CN,...
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SubjectTerms AGRICULTURE
ANIMAL HUSBANDRY
BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES
FISHING
FORESTRY
HUMAN NECESSITIES
HUNTING
HYGIENE
MEDICAL OR VETERINARY SCIENCE
PEST REPELLANTS OR ATTRACTANTS
PLANT GROWTH REGULATORS
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF
SPECIFIC USE OF COSMETICS OR SIMILAR TOILETPREPARATIONS
TRAPPING
Title Microbicidal active substances
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