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100646-51-3,MFCD09028086
Catalog No.:AA0002H9
100646-51-3 | Quizalofop-p-ethyl
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  • Technical Information
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  • Technical Information
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Technical Information
Catalog Number:
AA0002H9
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)[[email protected]](Oc1ccc(cc1)Oc1cnc2c(n1)ccc(c2)Cl)C
UNII:
1U4923B12R
Properties
Computed 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  

Synonyms
 
quizalofop-ethyl 
quizalofop-ethyl, (R)-isomer 
DPX-Y6202-31 
NCI-861094 
Ethyl (R)-2-(4-((6-chloro-2-quinoxalinyl)oxy)phenoxy)propanoate 
1U4923B12R 
ethyl (2R)-2-[4-(6-chloroquinoxalin-2-yl)oxyphenoxy]propanoate 
Propanoic acid, 2-[4-[(6-chloro-2-quinoxalinyl)oxy]phenoxy]-, ethyl ester, (2R)- 
(2R)-2-[4-[(6-chloro-2-quinoxalinyl)oxy]phenoxy]propanoic acid ethyl ester 
Targa D 
Propanoic acid, 2-(4-((6-chloro-2-quinoxalinyl)oxy)phenoxy)-, ethyl ester, (R)- 
C19H17ClN2O4 
quizalofop-ethyl, (S)-isomer 
Propanoic acid, 2-(4-((6-chloro-2-quinoxalinyl)oxy)phenoxy)-, ethyl ester, (2R)- 
Targa D+ 
(+)-quizalofop-ethyl 
(R)-Quizalofop Ethyl 
AC1LUTIB 
SCHEMBL53466 
Ethyl (R)-2-[4-(6-Chloroquinoxalin-2-yloxy)phenoxy]propionate 
Jsp000150 
CHEMBL3138620 
DTXSID0034857 
quizalofop-p-ethyl 
DPX-Y6202 
CHEBI:137938 
HY-B1950 
ZINC1854181 
MFCD09028086 
AKOS015895320 
CS-5264 
AN-34358 
AS-13056 
CJ-30604 
Quizalofop-p-ethyl 
LS-121324 
TL8000066 
FT-0631008 
A800251 
J-000190 
Quizalofop-p-ethyl, PESTANAL(R), analytical standard 
Ethyl (R)-2-[4-(6-chloro-2-quinoxalyloxy)phenoxy]propionate 
UNII-7280704RL4 component OSUHJPCHFDQAIT-GFCCVEGCSA-N 
ethyl (2R)-2-[4-(6-chloranylquinoxalin-2-yl)oxyphenoxy]propanoate 
ethyl (2R)-2-[4-(6-chloroquinoxalin-2-yloxy)phenoxy]propionate 
100646-51-3 
Ethyl (2R)-2-[4-[(6-Chloroquinoxalin-2-yl)oxy]phenoxy]propionate 
ethyl (2R)-2-{4-[(6-chloroquinoxalin-2-yl)oxy]phenoxy}propanoate 
Assure 
Quinofop-ethyl 
Xylofop-ethyl 
C19-H17-Cl-N2-O4 
CID1617113 
1ST22089 
H165 
Assure II 
Targa Super 
Quizalofop-P-ethyl [ISO] 
UNII-1U4923B12R 
Literature

Title: Molecular bases for resistance to acetyl-coenzyme A carboxylase inhibitor in Japanese foxtail (Alopecurus japonicus).

Journal: Pest management science 20120901

Title: Enantioselectivity in degradation and transformation of quizalofop-ethyl in soils.

Journal: Chirality 20120701

Title: Quizalofop-p-ethyl-induced phytotoxicity and genotoxicity in Lemna minor and Lemna gibba.

Journal: Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering 20120101

Title: Differential enantioselectivity of quizalofop ethyl and its acidic metabolite: direct enantiomeric separation and assessment of multiple toxicological endpoints.

Journal: Journal of hazardous materials 20110215

Title: Characterization of racemization of chiral pesticides in organic solvents and water.

Journal: Journal of chromatography. A 20100903

Title: Synthesis and biological activity of 4-(4,6-disubstituted-pyrimidin-2-yloxy)phenoxy acetates.

Journal: Molecules (Basel, Switzerland) 20100223

Title: Phosphate-solubilizing and plant-growth-promoting Pseudomonas aeruginosa PS1 improves greengram performance in quizalafop-p-ethyl and clodinafop amended soil.

Journal: Archives of environmental contamination and toxicology 20100201

Title: Toxicity assessment of herbicides quizalafop-p-ethyl and clodinafop towards Rhizobium pea symbiosis.

Journal: Bulletin of environmental contamination and toxicology 20090601

Title: Case report: mixed cholestatic/hepatocellular liver injury induced by the herbicide quizalofop-p-ethyl.

Journal: Environmental health perspectives 20071001

Title: [Potential use of the herbicide quizalofop-p-ethyl for eicosapentaenoic acid overproduction by the diatom Nitzschia laevis].

Journal: Sheng wu gong cheng xue bao = Chinese journal of biotechnology 20070901

Title: Development of an enzyme-linked immunosorbent assay for quantitative determination of quizalofop-p-ethyl.

Journal: Journal of agricultural and food chemistry 20061115

Title: Use of plant cell cultures to study graminicide effects on lipid metabolism.

Journal: Phytochemistry 20030701

Title: Enzyme inhibitors to increase poly-3-hydroxybutyrate production by transgenic tobacco.

Journal: Bioscience, biotechnology, and biochemistry 20021201

Title: Effects of water management and herbicide treatments on red rice control.

Journal: Mededelingen (Rijksuniversiteit te Gent. Fakulteit van de Landbouwkundige en Toegepaste Biologische Wetenschappen) 20020101

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