http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0453883-A2
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0efa077d881a96aeb1e29b21ef1bbb58 |
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S106-90 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-75 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-74 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-26 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-75 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-74 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C05G3-90 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-58 |
filingDate | 1991-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a29c6be2849b40fdf1c34972ada4cf9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8db79a3c7380ca2fe0bc59d4aae7ee37 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f21b61737c83a7c9c882164e7ad228f7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1a8a003342facfb37e300d1b2a628e18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_746d35de68222e676a3d2c021b8f0399 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9bca0bd4a88fcdae1fed1a68fec4bc64 |
publicationDate | 1991-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | EP-0453883-A2 |
titleOfInvention | 2-amino-4-trichloropyridine derivatives |
abstract | R¹ Wasserstoff oder C₁-C₈-Alkyl; R² C₁-C₈-Alkyl; C₅-C₈-Cycloalkyl; C₂-C₄-Alkenyl; gegebenenfalls substituiertes Phenyl, Benzyl oder Phenylsulfonyl; n-CX-R³, -SO₂R³ oder -PX(OR⁴)₂ oder R¹ und R² gemeinsam =CR⁵R⁶ oder -CO-Z-CO-, mit X Sauerstoff oder Schwefel, R³ C₁-C₂₀-Alkyl; C₂-C₆-Alkenyl; Amino; C₁-C₆-Alkylamino; Di-C₁-C₆-alkylamino; Morpholino; Piperidino; Pyrazolidino; C₁-C₈-Alkylcarbonylamino; gegebenenfalls substituiertes Phenylamino oder Benzylamino; ngegebenenfalls substituiertes Phenyl oder Heteroaryl; R⁴ C₁-C₈-Alkyl; C₁-C₈-Halogenalkyl oder gegebenenfalls substituiertes Phenyl; R⁵ Wasserstoff; C₁-C₄-Alkyl oder gegebenenfalls substituiertes Phenyl; R⁶ gegebenenfalls substituiertes Phenyl; Z gegebenenfalls substituiertes Ethylen, welches Teil eines gegebenenfalls substituierten Cycloalkyl- oder Cycloalkylenrestes sein kann; gegebenenfalls substituiertes Ethenylen, welches Teil eines gegebenenfalls substituierten aromatischen oder heteroaromatischen Ringes sein kann; nwobei Z nicht Teil eines unsubstituierten Phenylrestes ist, sowie deren landwirtschaftlich brauchbaren Salze, Verfahren zu ihrer Herstellung und ihre Verwendung als Nitrifikationsinhibitoren. 2-amino-4-trichloromethylpyridines of the general formula I in which the substituents have the following meaning: R¹ Hydrogen or C₁-C₈ alkyl; R² C₁-C₈ alkyl; C₅-C₈ cycloalkyl; C₂-C₄ alkenyl; optionally substituted phenyl, benzyl or phenylsulfonyl; -CX-R³, -SO₂R³ or -PX (OR⁴) ₂ or R1 and R2 together = CR⁵R⁶ or -CO-Z-CO-, with X Oxygen or sulfur, R³ C₁-C₂₀ alkyl; C₂-C₆ alkenyl; Amino; C₁-C₆ alkylamino; Di-C₁-C₆ alkylamino; Morpholino; Piperidino; Pyrazolidino; C₁-C₈ alkylcarbonylamino; optionally substituted phenylamino or benzylamino; optionally substituted phenyl or heteroaryl; R⁴ C₁-C₈ alkyl; C₁-C₈ haloalkyl or optionally substituted phenyl; R⁵ Hydrogen; C₁-C₄ alkyl or optionally substituted phenyl; R⁶ optionally substituted phenyl; Z optionally substituted ethylene, which can be part of an optionally substituted cycloalkyl or cycloalkylene radical; optionally substituted ethenylene, which can be part of an optionally substituted aromatic or heteroaromatic ring; where Z is not part of an unsubstituted phenyl radical, as well as their agriculturally useful salts, processes for their preparation and their use as nitrification inhibitors. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2762468-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2014131735-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103058781-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2014122065-A1 |
priorityDate | 1990-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 417.