105512-06-9 | Clodinafop-propargyl

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$34.00	$24.00
25g	98%	in stock	$158.00	$111.00

Description

• Catalog Number: AI06760
• Chemical Name: Clodinafop-propargyl
• CAS Number: 105512-06-9
• Molecular Formula: C17H13ClFNO4
• Molecular Weight: 349.7408
• MDL Number: MFCD01632328
• SMILES: C#CCOC(=O)[C@H](Oc1ccc(cc1)Oc1ncc(cc1F)Cl)C

Computed Properties

• Complexity: 461
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 24
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 7
• XLogP3: 3.9

Upstream Synthesis Route

The chemical compound (R)-Prop-2-yn-1-yl 2-(4-((5-chloro-3-fluoropyridin-2-yl)oxy)phenoxy)propanoate is a versatile reagent frequently employed in chemical synthesis processes. It plays a crucial role as a key building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials.In chemical synthesis, (R)-Prop-2-yn-1-yl 2-(4-((5-chloro-3-fluoropyridin-2-yl)oxy)phenoxy)propanoate serves as a valuable intermediate for the preparation of diverse compounds due to its unique chemical structure and functional groups. Its alkynyl group and substituted phenyl rings enable it to participate in a wide range of reactions, including cross-coupling reactions, nucleophilic substitutions, and condensation reactions.Furthermore, the presence of the chlorine and fluorine atoms in the compound provides opportunities for further functionalization and modification through selective transformations. This flexibility in chemical reactivity makes (R)-Prop-2-yn-1-yl 2-(4-((5-chloro-3-fluoropyridin-2-yl)oxy)phenoxy)propanoate a valuable tool for chemists and researchers seeking to synthesize complex molecules with specific properties and applications.

Literature

• Direct chiral resolution of cloquintocet-mexyl and its application to in vitro degradation combined with clodinafop-propargyl.

  Biomedical chromatography : BMC 20120901

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

  Pest management science 20120901

• Broad resistance to ACCase inhibiting herbicides in a ryegrass population is due only to a cysteine to arginine mutation in the target enzyme.

  PloS one 20120101

• Waterborne exposure to clodinafop-propargyl disrupts the posterior and ventral development of zebrafish embryos.

  Environmental toxicology and chemistry 20110701

• Using a selectivity index to evaluate logarithmic spraying in grass seed crops.

  Pest management science 20091101