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Picoxystrobin

CAS 117428-22-5Formula C18H16F3NO4MW 367.3PubChem 11285653

Picoxystrobin is a broad-spectrum strobilurin fungicide primarily used in agricultural and plant pathology research to study fungal disease control mechanisms and evaluate antifungal efficacy.

Loading RDKit molecule structure...
InChIKey: IBSNKSODLGJUMQ-SDNWHVSQSA-NC18H16F3NO4 | MW 367.3

Chemical Identity

Molecular Formula

C18H16F3NO4

Molecular Weight

367.3 g/mol

Exact Mass

367.103142

PubChem CID

11285653

IUPAC Name

methyl (E)-3-methoxy-2-[2-[[6-(trifluoromethyl)-2-pyridinyl]oxymethyl]phenyl]prop-2-enoate

SMILES String

CO/C=C(/C(=O)OC)c1ccccc1COc1cccc(C(F)(F)F)n1

Names & Synonyms

62DH7GEL1PCHEBI:83197methyl (2E)-3-methoxy-2-(2-(6-(trifluoromethyl)-2-pyridyloxymethyl)phenyl)acrylatemethyl (2E)-3-methoxy-2-{2-[6-(trifluoromethyl)-2-pyridyloxymethyl]phenyl}acrylatemethyl (alphaE)-alpha-(methoxymethylene)-2-(((6-(trifluoromethyl)-2-pyridinyl)oxy)methyl)benzeneacetate
Show all synonyms
methyl (alphaE)-alpha-(methoxymethylene)-2-[[[6-(trifluoromethyl)-2-pyridinyl]oxy]methyl]benzeneacetatePicoxystrobin [ISO]Methyl (E)-3-methoxy-2-[2-[[6-(trifluoromethyl)pyridin-2-yl]oxymethyl]phenyl]prop-2-enoate(E)-Methyl 3-methoxy-2-(2-(((6-(trifluoromethyl)pyridin-2-yl)oxy)methyl)phenyl)acrylatemethyl (2E)-3-methoxy-2-[2-({[6-(trifluoromethyl)pyridin-2-yl]oxy}methyl)phenyl]prop-2-enoateBenzeneacetic acid, alpha-(methoxymethylene)-2-[[[6-(trifluoromethyl)-2-pyridinyl]oxy]methyl]-, methyl ester, (alphaE)-Picoxystrobin (Standard)PICOXYSTROBIN [MI]Tox21_300625methyl (E)-3-methoxy-2-[2-[[6-(trifluoromethyl)-2-pyridyl]oxymethyl]phenyl]prop-2-enoate
External Identifiers
DTXSID9047542DTXCID7027542RefChem:174175UNII-62DH7GEL1PMFCD04112618SCHEMBL18977CHEMBL522759orb1692471SCHEMBL29377786MSK21131AKOS016011129EBC-367043HY-136355R

Catalog Overview

Picoxystrobin is a synthetic methoxyacrylate strobilurin fungicide. It functions by inhibiting mitochondrial respiration in fungi, specifically targeting the cytochrome bc1 complex (complex III) in the electron transport chain. This disruption prevents ATP synthesis, leading to the cessation of fungal growth and spore germination. In research settings, Picoxystrobin is utilized to investigate antifungal mechanisms, evaluate resistance development, and explore its efficacy against various plant pathogens.

Use Context

  • Research chemical sourcing
  • Custom synthesis and catalog availability review
  • COA, SDS, pricing, and fulfillment workflow

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

White crystalline solid

Physical State

Solid

Melting Point

75.0 °C

Boiling Point

380.0 °C

Density

1.28 g/cm³

Water Solubility

Very slightly soluble

Flash Point

219.9 °C

Applications / Classifications

Research intermediateCustom synthesis building block

Biological Target Reference

No verified biological target assignment. This compound is listed primarily as a research or synthetic intermediate.

Preliminary Safety-Style Reference

Preliminary

Preliminary safety-style information for reference only. Not a supplier SDS.

Handling and Storage
  • Handle with appropriate personal protective equipment (PPE) including gloves, eye protection, and a lab coat. Use in a well-ventilated area or fume hood. Avoid inhalation, ingestion, and skin contact. Refer to the Safety Data Sheet (SDS) for detailed hazard information and emergency procedures. Store in a cool, dry place away from incompatible materials.

Related Products / Graph Discovery

Related products, derivatives, keywords, and application cues for catalog discovery.

Related CAS / Similar Products

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Recommended application cues

Research intermediateCustom synthesis building block

Catalog discovery cues, not supplier-verified claims.

Related HS Code / Compliance

HS Code: 380892GHS Pictograms: GHS07, GHS09Shipment review: Shipment details require review before fulfillment.

Compliance cues are non-linked reference tags and require shipment review.

Catalog navigation

Related catalog entries

Other public CAS pages in this catalog. These links support navigation across additional intermediates and do not imply equivalence, availability, or shared use.

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