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Acynonapyr

CAS No.
1332838-17-1
Chemical Name:
Acynonapyr
Synonyms
Acynonapyr;(1R,3r,5S)-3-[2-propoxy-4-(trifluoromethyl)phenoxy]-9-{[5-(trifluoromethyl)pyridin-2-yl]oxy}-9-azabicyclo[3.3.1]nonane
CBNumber:
CB24745307
Molecular Formula:
C24H26F6N2O3
Molecular Weight:
504.47
MDL Number:
MOL File:
1332838-17-1.mol
Last updated:2026-07-31 15:25:15

Acynonapyr Properties

Boiling point 510.475±60.00 °C(Press: 760.00 Torr)(predicted)
Density 1.300±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
pka 1.048±0.10(predicted)
FDA UNII HG85ZH8U3V

SAFETY

Risk and Safety Statements

Symbol(GHS)  Environment (GHS09)
GHS09
Signal word  Warning
Hazard statements  H400
Precautionary statements  P273-P391-P501

Acynonapyr price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth HDC83817 Acynonapyr 1332838-17-1 10mg $1044.9 2026-06-04 Buy
Biosynth HDC83817 Acynonapyr 1332838-17-1 25mg $1622.5 2026-06-04 Buy
aablocks AA024KLM (3-endo)-3-[2-Propoxy-4-(trifluoromethyl)phenoxy]-9-[[5-(trifluoromethyl)-2-pyridinyl]oxy]-9-azabicyclo[3.3.1]nonane 1332838-17-1 10mg $659 2026-06-01 Buy
Product number Packaging Price Buy
HDC83817 10mg $1044.9 Buy
HDC83817 25mg $1622.5 Buy
AA024KLM 10mg $659 Buy

Acynonapyr Chemical Properties,Uses,Production

Description

Acynonapyr is an insecticide used to selectively control spider mite. Little has currently been published regarding its environmental fate and behaviour. Acynonapyr is toxic to fish. It is not highly toxic to mammals either via ingestion or in contact with the skin. It is reported to have developmental effects and may be a liver and kidney toxicant.

Uses

Acynonapyr is used in pesticidal compositions.

Production Methods

Acynonapyr is manufactured through an industrial process that brings together its pyridazinone core and the heavily substituted aryl side chain using a modular route designed to control regioselectivity and halogen based impurities. Production typically starts with building the pyridazinone scaffold from an appropriately substituted diester or diketone, followed by cyclisation and activation, often via chlorination, to make the heterocycle receptive to nucleophilic substitution. In a parallel stream, the fluorinated aromatic fragment is prepared through controlled halogenation and functionalisation to generate a suitably reactive electrophile. The key assembly step is coupling this activated aryl intermediate with the pyridazinone nucleus under anhydrous, base-mediated conditions that suppress over-alkylation and rearrangements.

Mechanism of action

Acts on inhibitory glutamate receptors and disrupts neurotransmission. Calcium-activated potassium channel (KCa2) modulator.

Pesticide Type

Insecticide; Acaricide

Acynonapyr Preparation Products And Raw materials

Raw materials

Preparation Products

Acynonapyr Suppliers

Global( 5)Suppliers
Supplier Tel Email Country ProdList Advantage
Shenzhen Regent Biochemical Technology Co., Ltd. 0755-85201366 18938635012 sales@regentsciences.com China 9385 58
Shaanxi Istare Biotechnology Co., Ltd. 18682931470; 18682931470 2142355700@qq.com China 4411 58
Shanghai Titan Scientific Co.,Ltd 18616708014 yhx@titansci.com China 9999 58

Related articles

  • How to synthesize Acynonapyr?
  • Acynonapyr is effective against spider mites, such as Tetranychus urticae (two-spotted spider mite) and Panonychus ulmi (Europ....
  • Feb 26,2024
(1R,3r,5S)-3-[2-propoxy-4-(trifluoromethyl)phenoxy]-9-{[5-(trifluoromethyl)pyridin-2-yl]oxy}-9-azabicyclo[3.3.1]nonane Acynonapyr 1332838-17-1