Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H5Cl2NO2 |
Molecular Weight | 242.058 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=C(Cl)C=CC2=C1N=CC(Cl)=C2
InChI
InChIKey=FFSSWMQPCJRCRV-UHFFFAOYSA-N
InChI=1S/C10H5Cl2NO2/c11-6-3-5-1-2-7(12)8(10(14)15)9(5)13-4-6/h1-4H,(H,14,15)
Approval Year
PubMed
Title | Date | PubMed |
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Cyanobacteria in Uruguayan rice fields: diversity, nitrogen fixing ability and tolerance to herbicides and combined nitrogen. | 2001 Oct 4 |
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Auxin herbicides induce H(2)O(2) overproduction and tissue damage in cleavers (Galium aparine L.). | 2001 Sep |
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On the mechanism of selectivity of the corn herbicide BAS 662H: a combination of the novel auxin transport inhibitor diflufenzopyr and the auxin herbicide dicamba. | 2002 Oct |
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Influences of quinclorac on culturable microorganisms and soil respiration in flooded paddy soil. | 2003 Dec |
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Phylogenetic and degradation characterization of Burkholderia cepacia WZ1 degrading herbicide quinclorac. | 2003 Nov |
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3,7-Dichloro-quinoline-8-carboxylic acid. | 2008 Aug 20 |
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Influence of simulated Quinclorac drift on the accumulation and movement of herbicide in tomato (Lycopersicon esculentum) plants. | 2009 Jul 22 |
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EPA PESTICIDE CODE |
128974
Created by
admin on Fri Dec 15 18:11:42 GMT 2023 , Edited by admin on Fri Dec 15 18:11:42 GMT 2023
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Quinclorac
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3J06V625EE
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quinclorac
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84087-01-4
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81974
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91739
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DTXSID6032641
Created by
admin on Fri Dec 15 18:11:42 GMT 2023 , Edited by admin on Fri Dec 15 18:11:42 GMT 2023
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PRIMARY |
SUBSTANCE RECORD