100646-51-3 | Quizalofop-p-ethyl

Packsize	Purity	Availability	Price	Discounted Price
25mg	98%	in stock	$65.00	$46.00
100mg	98%	in stock	$97.00	$68.00
500mg	98%	in stock	$239.00	$167.00
1g	98%	in stock	$444.00	$311.00

Description

• Catalog Number: AA03113
• Chemical Name: Quizalofop-p-ethyl
• CAS Number: 100646-51-3
• Molecular Formula: C19H17ClN2O4
• Molecular Weight: 372.8023
• MDL Number: MFCD09028086
• SMILES: CCOC(=O)[C@H](Oc1ccc(cc1)Oc1cnc2c(n1)ccc(c2)Cl)C

Computed Properties

• Complexity: 459
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 26
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 7
• XLogP3: 4.3

Upstream Synthesis Route

Quizalofop-p-ethyl is a herbicide commonly used in agricultural practices for its potent ability to selectively control grass weeds in various crops. In chemical synthesis, this active ingredient serves as a crucial building block for the development of herbicidal formulations and derivatives with improved efficacy and environmental safety. By incorporating Quizalofop-p-ethyl into synthetic pathways, chemists can create innovative herbicidal compounds designed to target specific weed species while minimizing harm to desirable plants and the surrounding ecosystem. This compound's versatility and effectiveness in weed management make it a valuable tool in the field of chemical synthesis for sustainable agricultural practices.

Literature

• 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