http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-465866-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N37-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-54
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P3-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-54
filingDate 1978-01-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1979-01-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-465866-A1
titleOfInvention A PROCEDURE FOR THE PREPARATION OF NEW N- (3,5-DIHA- LOFENYL) SUCCINIMIDES
abstract This invention relates to N- (3,5, -dihalophenyl-alpha-spirocycloalkanesuccinimides of formula ** (Formula) ** Where X is a chlorine or bromine atom and R is a C3-C6 alkylene group (eg trimethylene, tetramethylene , pentamethylene, methylpentamethylene, hexamethylene) and their preparation and use It is already known that some of the derivatives of N- (3,5-dihalophenyl) succinimide, whose alpha and / or beta positions optionally substituted with various substituents, exert antimicrobial activity on Certain microorganisms. It has now been found that N- (3,5-dihalophenyl) succinimides (I) with a spirocycloalkane group in the alpha position have a markedly higher antifungal activity than their homologues and also do not present material phytotoxicity to plants (e.g. rice, bean, adzuki bean, soybean, potato, tobacco, cucumber, tomato, pea, eggplant, bell pepper, beans, melon, lettuce, onion, watermelon, strawberry, radish, cabbage, Chinese cabbage, apple, pear, grape, peach and Japanese apricot).
priorityDate 1977-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 22.