trifluenfuronate

Chinese: 三氟杀线酯; French: (n.f.)Russian:


Status: ISO 1750 (provisionally approved)
IUPAC PIN: mixture of 60–80% rac-3,4,4-trifluorobut-3-en-1-yl (2R,3R)-2-(2-methoxyphenyl)-5-oxooxolane-3-carboxylate and 40–20% of the rac-(2R,3S)-isomers
IUPAC name: mixture of 60–80% trans-isomers 3,4,4-trifluorobut-3-enyl (2RS,3RS)-2-(2-methoxyphenyl)-5-oxotetrahydrofuran-3-carboxylate and 40–20% of the cis-isomers 3,4,4-trifluorobut-3-enyl (2RS,3SR)-2-(2-methoxyphenyl)-5-oxotetrahydrofuran-3-carboxylate
1979 Rules:
mixture of 60–80% trans-isomers 3,4,4-trifluorobut-3-enyl (2RS,3RS)-tetrahydro-2-(2-methoxyphenyl)-5-oxofuran-3-carboxylate and 40–20% of the cis-isomers 3,4,4-trifluorobut-3-enyl (2RS,3SR)-tetrahydro-2-(2-methoxyphenyl)-5-oxofuran-3-carboxylate
CAS name: 3,4,4-trifluoro-3-buten-1-yl tetrahydro-2-(2-methoxyphenyl)-5-oxo-3-furancarboxylate
CAS Reg. No.: 2074661-82-6
Formula: C16H15F3O5
Activity: acaricides (unclassified acaricides)
nematicides (fluoroalkenyl nematicides)
Notes: The names sanfoshaxianzhi and Trifluorocide have been used in the literature. The mixture of 2 trans-isomers has the CAS Registry Number 2094595-23-8.
Structure: Structural formula of trifluenfuronate
Pronunciation: trī-floo-ěn-fūr-ǒn-āt  Guide to British pronunciation
InChIKey: VDQRIZJOECVEPJ-UHFFFAOYSA-N
InChI: InChI=1S/C16H15F3O5/c1-22-12-5-3-2-4-9(12)14-10(8-13(20)24-14)16(21)23-7-6-11(17)15(18)19/h2-5,10,14H,6-8H2,1H3

A data sheet from the Compendium of Pesticide Common Names