361366-15-6

Basic information

• Product Name: ethyl 1-{[(2,4,6-trimethylphenyl)acetyl]oxy}cyclopentanecarboxylate
• Synonyms: Ethyl 1-(2-mesitylacetoxy)cyclopentanecarboxylate
• CAS NO: 361366-15-6
• Molecular Formula: C₁₉H₂₆O₄
• Molecular Weight: 318.4073
• EINECS: 609-205-5
• Mol File: 361366-15-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 414.5°C at 760 mmHg
• Flash Point: 200.1°C
• Density: 1.09g/cm³
• Vapor Pressure: 4.44E-07mmHg at 25°C
• Refractive Index: 1.524
• CAS DataBase Reference: ethyl 1-{[(2,4,6-trimethylphenyl)acetyl]oxy}cyclopentanecarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 1-{[(2,4,6-trimethylphenyl)acetyl]oxy}cyclopentanecarboxylate(361366-15-6)
• EPA Substance Registry System: ethyl 1-{[(2,4,6-trimethylphenyl)acetyl]oxy}cyclopentanecarboxylate(361366-15-6)

Safety Data

• Hazardous Substances Data: 361366-15-6(Hazardous Substances Data)

Upstream product

• 16841-19-3 1-hydroxy-cyclopentanecarboxylic acid 
• 120-92-3 cyclopentanone 
• 5117-85-1 1-hydroxycyclopentanecarbonitrile 
• 52629-46-6 (2,4,6-trimethyl-phenyl)acetyl chloride 
• 41248-23-1 hydroxycyclopentanecarboxylic acid ethyl ester 

Downstream Products

• 1350443-99-0 C₂₈H₂₈F₃NO₅ 
• 1350443-98-9 C₂₇H₂₈BrNO₅ 
• 1350443-97-8 C₂₉H₃₃NO₅ 
• 1350443-96-7 C₂₇H₂₉NO₅ 
• 1350443-95-6 C₂₆H₂₇NO₅ 
• 1350443-94-5 C₂₃H₂₇NO₅ 
• 1350443-93-4 C₂₄H₂₉NO₅ 
• 1350443-91-2 C₂₃H₂₉NO₅ 
• 1350443-90-1 C₂₉H₃₂O₆ 
• 1350443-89-8 C₂₅H₂₃ClO₆ 
• 1350443-88-7 C₂₅H₂₄O₆ 
• 1350443-87-6 C₂₂H₂₂O₆ 
• 1350443-86-5 C₂₁H₂₄O₆ 
• 283594-90-1 spiromesifen 

Relevant articles and documents

Spirodiclofen and spiromesifen - Novel acaricidal and insecticidal tetronic acid derivatives with a new mode of action

The broad spectrum acaricides spirodiclofen (BAJ2740, trade name: Envidor) and spiromesifen (BSN2060, trade name: Oberon) with an additional excellent activity against whiteflies, both belong to the new chemical class of tetronic acid derivatives discovered at Bayer CropScience during the 1990s. The discovery process starting from herbicidal PPO (protoporphyrinogen oxidase) chemistry, the synthetic routes leading to the products, and some insight into process development of central intermediates is given. Spirodiclofen and spiromesifen have a new mode of action (interference with lipid biosynthesis), show no cross-resistance to any resistant mite or whitefly field population and are therefore valuable tools for resistance management.