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1477919-27-9

1477919-27-9 Structure

1477919-27-9 Structure
IdentificationBack Directory
[Name]

tyclopyrazoflor
[CAS]

1477919-27-9
[Synonyms]

tyclopyrazoflor
Propanamide, N-[3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)thio]-
[Molecular Formula]

C16H18ClF3N4OS
[MDL Number]

MFCD31746909
[MOL File]

1477919-27-9.mol
[Molecular Weight]

406.85
Chemical PropertiesBack Directory
[Boiling point ]

517.3±50.0 °C(Predicted)
[density ]

1.36±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[pka]

2.55±0.12(Predicted)
[color ]

White to off-white
[EPA Substance Registry System]

Propanamide, N-[3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)thio]- (1477919-27-9)
Hazard InformationBack Directory
[Uses]

Tyclopyrazoflor is an anthranilamide compound with pesticidal activity.
[Definition]

ChEBI: Tyclopyrazoflor is a member of the class of pyrazoles that is 1H-pyrazole which is substituted at positions 1, 3 and 4 by a pyridin-3-yl group, chloro group and an ethyl{3-[(3,3,3-trifluoropropyl)sulfanyl]propanoyl}nitrilo group, respectively. It is an insecticide from Dow AgroSciences LLC. It has a role as an insecticide. It is an organofluorine compound, a member of pyrazoles, a member of pyridines, a tertiary carboxamide, an organic sulfide and an organochlorine compound.
[Production Methods]

Tyclopyrazoflor is produced commercially through a process that begins with a [3+2] cyclization of 3-hydrazinopyridine hydrochloride and methyl acrylate to form a pyrazolidinone, followed by chlorination and oxidation to a disubstituted pyrazole. Regioselective nitration, reduction to the aminopyrazole, and acylation with 3-((3,3,3-trifluoropropyl)thio)propanoyl chloride yield a secondary amide intermediate, which is then alkylated to the final product. Key innovations include a thiol-ene reaction for the trifluoropropyl thioester precursor, achieving high regioselectivity using a benzoyl peroxide/N,N-dimethylaniline initiator system at low temperatures in semibatch mode, and an Ullmann coupling of N-(3-chloro-1H-pyrazol-4-yl)acetamide with 3-bromopyridine, catalysed by copper(I) chloride and 1,2-dimethylethylenediamine.
[Mechanism of action]

Unclear but thought to interfer with an insect's nervous system, specifically its neurotransmission, interacting with the chordotonal TRPV channels
[References]

[1] WO 2017140563 A1.
[Pesticide Type]

Insecticide
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