Home Other Building Blocks Quizalofop-p-ethyl

Quizalofop-p-ethyl

CAS No.:
100646-51-3
Catalog Number:
AG0002K1
Molecular Formula:
C19H17ClN2O4
Molecular Weight:
372.8023
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
25mg
96%(HPLC)powder
In Stock USA
United States
$73
- +
100mg
96%(HPLC)powder
In Stock USA
United States
$103
- +
500mg
96%(HPLC)powder
In Stock USA
United States
$228
- +
1g
96%(HPLC)powder
In Stock USA
United States
$408
- +
Product Description
Catalog Number:
AG0002K1
Chemical Name:
Quizalofop-p-ethyl
CAS Number:
100646-51-3
Molecular Formula:
C19H17ClN2O4
Molecular Weight:
372.8023
MDL Number:
MFCD09028086
IUPAC Name:
ethyl (2R)-2-[4-(6-chloroquinoxalin-2-yl)oxyphenoxy]propanoate
InChI:
InChI=1S/C19H17ClN2O4/c1-3-24-19(23)12(2)25-14-5-7-15(8-6-14)26-18-11-21-17-10-13(20)4-9-16(17)22-18/h4-12H,3H2,1-2H3/t12-/m1/s1
InChI Key:
OSUHJPCHFDQAIT-GFCCVEGCSA-N
SMILES:
CCOC(=O)[C@H](Oc1ccc(cc1)Oc1cnc2c(n1)ccc(c2)Cl)C
UNII:
1U4923B12R
Properties
Complexity:
459  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
372.088g/mol
Formal Charge:
0
Heavy Atom Count:
26  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
372.805g/mol
Monoisotopic Mass:
372.088g/mol
Rotatable Bond Count:
7  
Topological Polar Surface Area:
70.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.3  
Literature
Title Journal
Molecular bases for resistance to acetyl-coenzyme A carboxylase inhibitor in Japanese foxtail (Alopecurus japonicus). Pest management science 20120901
Enantioselectivity in degradation and transformation of quizalofop-ethyl in soils. Chirality 20120701
Quizalofop-p-ethyl-induced phytotoxicity and genotoxicity in Lemna minor and Lemna gibba. Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering 20120101
Differential enantioselectivity of quizalofop ethyl and its acidic metabolite: direct enantiomeric separation and assessment of multiple toxicological endpoints. Journal of hazardous materials 20110215
Characterization of racemization of chiral pesticides in organic solvents and water. Journal of chromatography. A 20100903
Synthesis and biological activity of 4-(4,6-disubstituted-pyrimidin-2-yloxy)phenoxy acetates. Molecules (Basel, Switzerland) 20100223
Phosphate-solubilizing and plant-growth-promoting Pseudomonas aeruginosa PS1 improves greengram performance in quizalafop-p-ethyl and clodinafop amended soil. Archives of environmental contamination and toxicology 20100201
Toxicity assessment of herbicides quizalafop-p-ethyl and clodinafop towards Rhizobium pea symbiosis. Bulletin of environmental contamination and toxicology 20090601
Case report: mixed cholestatic/hepatocellular liver injury induced by the herbicide quizalofop-p-ethyl. Environmental health perspectives 20071001
[Potential use of the herbicide quizalofop-p-ethyl for eicosapentaenoic acid overproduction by the diatom Nitzschia laevis]. Sheng wu gong cheng xue bao = Chinese journal of biotechnology 20070901
Development of an enzyme-linked immunosorbent assay for quantitative determination of quizalofop-p-ethyl. Journal of agricultural and food chemistry 20061115
Use of plant cell cultures to study graminicide effects on lipid metabolism. Phytochemistry 20030701
Enzyme inhibitors to increase poly-3-hydroxybutyrate production by transgenic tobacco. Bioscience, biotechnology, and biochemistry 20021201
Effects of water management and herbicide treatments on red rice control. Mededelingen (Rijksuniversiteit te Gent. Fakulteit van de Landbouwkundige en Toegepaste Biologische Wetenschappen) 20020101
Properties