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Fluensulfone

Fluensulfone Suppliers list
Company Name: Wuhan Augda Biotechnology Co., Ltd  Gold
Tel: 15071299552
Email: 262933239@qq.com
Company Name: Wuhan Yingnuo Pharmaceutical Technology Co., Ltd.  Gold
Tel: +86-027-59232304 15387063101
Email: 1276242629@qq.com
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Chemsky (shanghai) International Co.,Ltd  
Tel: 021-50135380
Email: shchemsky@sina.com
Company Name: Shanghai TaoSu Biochemical Technology Co., Ltd.  
Tel: 021-33632979
Email: info@tsbiochem.com

Fluensulfone manufacturers

  • Fluensulfone
  • Fluensulfone pictures
  • $35.00
  • 2026-05-11
  • CAS:318290-98-1
  • Purity: 98.57%
  • Supply Ability: 10g
  • Fluensulfone
  • Fluensulfone pictures
  • $1.00
  • 2019-09-06
  • CAS:318290-98-1
  • Min. Order: 1KG
  • Purity: 95%~99%

Related articles

Fluensulfone Basic information
Product Name:Fluensulfone
Synonyms:5-Chloro-2-[(3,4,4-trifluoro-3-buten-1-yl)sulfonyl]thiazole;5-Chloro-2-[(3,4,4-trifluorobut-3-en-1-yl)sulfonyl]-1,3-thiazole;Fluensulfone;5-chloro-2-(3,4,4-trifluorobut-3-enylsulfonyl)thiazole;5-Chloro-2-[(3,4,4-trifluoro-3-buten-1-yl)sulfonyl]-1,3-thiazole;6-[2-(TERT-BUTOXYCARBONYLAMINO)ETHYLAMINO]-7-CHLORO-1-CYCLOPROPYL-4-OXO-QUINOLINE-3-CARBOXYLIC ACID;5-Chloro-2-((3,4,4-trifluorobut-3-en-1-yl)sulfonyl)thiazole;Fluensulfone Solution, 100ppm
CAS:318290-98-1
MF:C7H5ClF3NO2S2
MW:291.7
EINECS:
Product Categories:Agro-Products, Heterocycles, Sulfur & Selenium Compounds
Mol File:318290-98-1.mol
Fluensulfone Structure
Fluensulfone Chemical Properties
Melting point 34 °C
Boiling point 375.5±52.0 °C(Predicted)
density 1.577±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility soluble in organic solvents such as ethanol, DMSO, and dimethyl formamide.
pka-3.12±0.10(Predicted)
form A crystalline solid
Henry's Law Constant6.1×101 mol/(m3Pa) at 25℃, Ebert et al. (2023)
InChIInChI=1S/C7H5ClF3NO2S2/c8-5-3-12-7(15-5)16(13,14)2-1-4(9)6(10)11/h3H,1-2H2
InChIKeyXSNMWAPKHUGZGQ-UHFFFAOYSA-N
SMILESS1C(Cl)=CN=C1S(CC/C(/F)=C(/F)\F)(=O)=O
EPA Substance Registry SystemThiazole, 5-chloro-2-[(3,4,4-trifluoro-3-buten-1-yl)sulfonyl]- (318290-98-1)
color Yellow coloured resin-like
Safety Information
MSDS Information
Fluensulfone Usage And Synthesis
DescriptionFluensulfone is an agricultural and horticultural nematicide. It has a moderate oral toxicity and low by dermal and inhalation routes. It is an irritant and skin sensitiser. It can be expected to dissipate rather rapidly in the environment and has a low to moderate toxicity to fauna and flora.
Chemical PropertiesFluensulfone is a yellow coloured resin-like solid with a charcateristic odour. It is soluble in organic solvents such as ethanol, DMSO, and dimethyl formamide. The solubility of fluensulfone in these solvents is approximately 30 mg/ml. fluensulfone is a non-fumigant nematicide containing sulfone, thiazolyl and fluoroalkenyl functional groups.
UsesFluensulfone is used as nematicide.
DefinitionChEBI: Fluensulfone is a member of the class of 1,3-thiazoles carrying 3,4,4-trifluorobut-3-ene-1-sulfonyl and chloro substituents at positions 2 and 5 respectively. A nematicide that is effective against a number of plant parasitic nematodes in a range of agricultural and horticultural crops. It has a role as a nematicide and an agrochemical. It is a member of 1,3-thiazoles, an organochlorine pesticide, a sulfone, an organofluorine pesticide and an olefinic compound.
ApplicationThe application of fluensulfone substantially reduced nematode multiplication either in tomato or cucumber cultivation at all doses above 24 ml 100 m.1. Plants cultivated in plots treated with fluensulfone produced significantly more fruits throughout the cropping season for both crops.
Production MethodsCommercial production of fluensulfone follows a sequence built around constructing a heterocyclic thioether, converting it to the corresponding sulfoxide or sulfone, and introducing the fluoroalkenyl side chain. The key industrial step is the dehalogenation of a di halogenated fluoroalkyl intermediate to generate the characteristic CF=CF2 moiety. Upstream, manufacturers prepare a thiazole based thioether precursor, then oxidise it under controlled conditions using an oxidant and a metal oxide catalyst to obtain the sulfone.
Mode of actionFluensulfone is a new chemical class of nematicide whose mechanism of action is inhibits development, egg-laying, egg-hatching, feeding and locomotion.
Pesticide TypeNematicide
Fluensulfone Preparation Products And Raw materials
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