http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-101863-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_648c9679dd9ec36125406a2dafa6bf7e |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-88 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-707 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N37-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N37-18 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-74 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-707 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-88 |
| filingDate | 2015-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8c3bcb7588daf6bd47dd5595d09c2ec http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7f9efd1308db80cbeba19aba2541a3a0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5065658e3bc7ea5c08468dd092d90964 |
| publicationDate | 2017-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-101863-A1 |
| titleOfInvention | SYNERGIC CONTROL OF WEEDS FROM APPLICATIONS OF HERBICIDES OF CARBOXYL PIRIDIN ACID AND PHOTOSYSTEM II INHIBITORS |
| abstract | Claim 1: A herbicidal composition containing a herbicidally effective synergistic amount of (a) a carboxylic acid pyridine herbicide or an agriculturally acceptable N-oxide, salt, or ester thereof, and b) a photosystem II inhibitor, or a salt or an agriculturally acceptable ester thereof, wherein the pyridine carboxylic acid herbicide contains a compound defined by the formula (1) in which X is N or Cl, in which Y is hydrogen, halogen, C₁₋₃ alkyl , C₁₋₃ haloalkyl, C₁₋₃ alkoxy, C₁₋₃ haloalkoxy, C₁₋₃ alkylthio or C₁₋₃ haloalkylthio; R¹ is OR¹ or NR¹R¹, wherein R¹ is hydrogen, C₁₋₈ alkyl, or C₇₋₁₀ arylalkyl, and R¹ and R¹ are independently hydrogen, C₁₋₁₂ alkyl, C₃₋₁₂ alkenyl, or C₃₋₁₂ alkynyl; R² is halogen, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₂₋₄ alkenyl, C₂₋₄ haloalkenyl, C₂₋₄ alkynyl, C₁₋₄ alkoxy, C₁₋₄ haloalkoxy, C₁₋₄ alkylthio, C₁₋₄ haloalkylthio, amino , C₁₋₄ alkylamino, C₂₋₄ haloalkylamino, formyl, C₁₋₃ alkylcarbonyl, C₁₋₃ haloalkylcarbonyl, cyano, or a group of the formula -CR¹⁷-CR¹⁸-SiR¹⁹R²⁰R²¹, wherein R¹⁷ is hydrogen, F, or Cl; R¹⁸ is hydrogen, F, Cl, C₁₋₄ alkyl, or C₁₋₄ haloalkyl; and R¹⁹, R²⁰ and R²¹ are independently, C₁₋₁₀ alkyl, C₃₋₆ cycloalkyl, phenyl, substituted phenyl, C₁₋₁₀ alkoxy, or OH; R³ and R⁴ are independently hydrogen, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₃₋₆ alkenyl, C₃₋₆ haloalkenyl, C₃₋₆ alkynyl, formyl, C₁₋₃ alkylcarbonyl, C₁₋₃ haloalkylcarbonyl, C₁₋₆ alkoxycarbonyl, C₁ ₋₆ alkylcarbamyl, C₁₋₆ alkylsulfonyl, C₁₋₆ trialkylsilyl, C₁₋₆ dialkylphosphonyl, or R³ and R⁴ taken together with N are a saturated ring of 5 or 6 members, or R³ and R⁴ taken together represent = CR³ (R⁴), wherein R³ and R⁴ are independently hydrogen, C₁₋₆ alkyl, C₃₋₆ alkenyl, C₃₋₆ alkynyl, C₁₋₆ alkoxy or C₃₋₆ alkylamino, or R³ and R⁴ taken together with = C represent a saturated ring of 5 or 6 members; A is one of the compounds A1 through A36 of the group of formulas (2); halocyclopropyl, C₂₋₄ alkenyl, C₂₋₄ haloalkenyl, C₂₋₄ alkynyl, C₁₋₃ alkoxy, C₁₋₃ haloalkoxy, C₁₋₃ alkylthio C₁₋₃ haloalkylthio, amino, C₁₋₄ alkylamino, C₂₋₄ haloalkylamino, OH, or CN; R⁶, R⁶, and R⁶, if applicable to group A, are independently hydrogen, halogen, C₁₋₄ alkyl, C₁₋₄ haloalkyl, cyclopropyl, halocyclopropyl, C₂₋₄ alkenyl, C₂₋₄ haloalkenyl, C₂₋₄ alkynyl, C₁ ₋₃ alkoxy, C₁₋₃ haloalkoxy, C₁₋₃ alkylthio, C₁₋₃ haloalkylthio, amino, C₁₋₄ alkylamino or C₂₋₄ haloalkylamino, OH, CN, or NO₂; R⁷ and R⁷ are independently hydrogen, halogen, C₁₋₄ alkyl, C₁₋₄ haloalkyl, cyclopropyl, halocyclopropyl, C₂₋₄ alkenyl, C₂₋₄ haloalkenyl, C₂₋₄ alkynyl, C₁₋₃ alkoxy, C₁₋₃ haloalkoxy, C₁₋ ₃ alkylthio, C₁₋₃ haloalkylthio, amino, C₁₋₄ alkylamino, C₁₋₄ haloalkylamino, or phenyl; R⁸ is hydrogen, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₃₋₆ alkenyl, C₃₋₆ haloalkenyl, C₃₋₆ alkynyl, formyl, C₁₋₃ alkylcarbonyl, C₁₋₃ haloalkylcarbonyl, C₁₋₆ alkoxycarbonyl, C₁₋ ₆ alkylcarbamyl, C₁₋₆ alkylsulfonyl, C₁₋₆ trialkylsilyl, or phenyl; or an N-oxide or an agriculturally acceptable salt thereof. Claim 20: The composition of any one of claims 1-19, which further contains an agriculturally acceptable adjuvant or vehicle. Claim 25: A method of controlling undesirable vegetation comprising applying to the vegetation or an area adjacent to the vegetation or applying to the soil or water, to control the outbreak or growth of the vegetation an effective herbicidal amount of: (a) a pyridine carboxylic acid herbicide containing a compound defined by the formula (1) in which X is N or Cl, wherein Y is hydrogen, halogen, C₁₋₃ alkyl, C₁₋₃ haloalkyl, C₁₋₃ alkoxy, C₁₋₃ haloalkoxy, C₁₋₃ alkylthio or C₁₋₃ haloalkylthio; R¹ is OR¹ or NR¹R¹, wherein R¹ is hydrogen, C₁₋₈ alkyl, or C₇₋₁₀ arylalkyl, and R¹ and R¹ are independently hydrogen, C₁₋₁₂ alkyl, C₃₋₁₂ alkenyl, or C₃₋₁₂ alkynyl; R² is halogen, C₁₋₄ alkyl, C₁₋₄, haloalkyl, C₂₋₄, alkenyl, C₂₋₄ haloalkenyl, C₂₋₄ alkynyl, C₁₋₄ alkoxy, C₁₋₄ haloalkoxy, C₁₋₄ alkylthio, C₁₋₄ haloalkylthio , amino, C₁₋₄ alkylamino, C₂₋₄ haloalkylamino, formyl, C₁₋₃ alkylcarbonyl, C₁₋₃ haloalkylcarbonyl, cyano, or a group of the formula -CR¹⁷ = CR¹⁸-SiR¹⁹R²⁰R²¹, in which R¹⁷ is hydrogen, F, or Cl; R¹⁸ is hydrogen, F, Cl, C₁₋₄ alkyl, or C₁₋₄ haloalkyl; and R¹⁹, R²⁰ and R²¹ are independently C₁₋₁₀ alkyl, C₁₋₆ cycloalkyl, phenyl, substituted phenyl, C₁₋₁₀ alkoxy, or OH; R³ and R⁴ are independently hydrogen, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₃₋₆ alkenyl, C₃₋₆ haloalkenyl, C₃₋₆ alkynyl formyl, C₁₋₃ alkylcarbonyl, C₁₋₃ haloalkylcarbonyl, C₁₋₆ alkoxycarbonyl, C₁₋ ₆ alkylcarbamyl, C₁₋₆ alkylsulfonyl, C₁₋₆ trialkylsilyl, C₁₋₆ dialkylphosphonyl, or R³ and R⁴ taken together with a saturated ring of 5 or 6 members, or R³ and R⁴ taken together represent = CR³ (R⁴), in which R³ and R⁴ are independently hydrogen, C₁₋₆ alkyl, C₃₋₆ alkenyl, C₃₋₆ alkynyl, C₃₋₆ alkoxy or C₁₋₆ alkylamino, or, R³ and R⁴ taken together with = C represent a saturated ring of 5 or 6 members; A is one of the groups A1 to A36; R⁵, if applicable to group A, is hydrogen, halogen, C₁₋₄ alkyl, C₁₋₄ haloalkyl, cyclopropyl, halocyclopropyl, C₂₋₄ alkenyl, C₂₋₄ haloalkenyl, C₂₋₄ alkynyl, C₁₋₃ alkoxy, C₁₋ ₃ haloalkoxy, C₁₋₃ alkylthio, C₁₋₃ haloalkylthio, amino, C₁₋₄ alkylamino, C₂₋₄ haloalkylamino, OH, or CN; R⁶, R⁶ and R⁶, if applicable to group A, are independently hydrogen, halogen, C₁₋₄ alkyl, C₁₋₄ haloalkyl, cyclopropyl, halocyclopropyl, C₂₋₄ alkenyl, C₂₋₄ haloalkenyl, C₂₋₄ alkynyl, C₁₋ ₃ alkoxy, C₁₋₃ haloalkoxy, C₁₋₃ alkylthio, C₁₋₃ haloalkylthio, amino, C₁₋₄ alkylamino or C₂₋₄ haloalkylamino, OH, CN, or NO₂; R⁷ and R⁷ are independently hydrogen, halogen, C₁₋₄ alkyl, C₁₋₄ haloalkyl, cyclopropyl, halocyclopropyl, C₂₋₄ alkenyl, C₂₋₄ haloalkenyl, C₂₋₄ alkynyl, C₁₋₃ alkoxy, C₁₋₃ haloalkoxy, C₁₋ ₃ alkylthio, C₁₋₃ haloalkylthio, amino, C₁₋₄ alkylamino, C₁₋₄ haloalkylamino, or phenyl; R⁸ is hydrogen, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₃₋₆ alkenyl, C₃₋₆ haloalkenyl, C₃₋₆ alkynyl, formyl, C₁₋₃ alkylcarbonyl, C₁₋₃ haloalkylcarbonyl, C₁₋₆ alkoxycarbonyl, C₁₋ ₆ alkylcarbamyl, C₁₋₆ alkylsulfonyl, C₁₋₆ trialkylsilyl, or phenyl; or an N-oxide or an agriculturally acceptable salt thereof; and (b) a photosystem II inhibitor, or an agriculturally acceptable salt or ester thereof. Claim 52: The method of any one of claims 25-51, which further contains an agriculturally acceptable adjuvant or vehicle. Claim 54: The method of any one of claims 25-53, wherein undesirable vegetation is controlled with a culture tolerant to glyphosate, glufosinate, dicamba, phenoxy auxin, pyridyloxy auxin, aryloxyphenoxypropionate, inhibitor of acetyl CoA carboxylase (ACCase), to imidazolinone, to acetolactate synthase (ALS) inhibitor, to 4-hydroxyphenyl pyruvate dioxygenase (HPPD) inhibitor, or to protoporphyrinogen oxidase (PPO) inhibitor. Claim 55: The method of claim 54, wherein the tolerant culture has multiple traits or stacked features that confer tolerance to multiple herbicides or multiple modes of action. Claim 57: The method of any of claims 25-56, wherein the undesirable vegetation contains a weed resistant or tolerant to a herbicide. Claim 58: The method of claim 57, wherein the tolerant resistant weed is a biotype with resistance or tolerance to multiple herbicides, multiple chemical classes, or multiple modes of herbicide action. |
| priorityDate | 2014-09-15-04:00^^<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: 577.