fluensulfone
Modify Date: 2024-01-05 10:53:00
fluensulfone structure
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Common Name | fluensulfone | ||
|---|---|---|---|---|
| CAS Number | 318290-98-1 | Molecular Weight | 291.698 | |
| Density | 1.6±0.1 g/cm3 | Boiling Point | 375.5±52.0 °C at 760 mmHg | |
| Molecular Formula | C7H5ClF3NO2S2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 180.9±30.7 °C | |
Use of fluensulfoneFluensulfone is a new nematicide for chemical control of plant parasitic nematodes. |
| Name | fluensulfone |
|---|---|
| Synonym | More Synonyms |
| Description | Fluensulfone is a new nematicide for chemical control of plant parasitic nematodes. |
|---|---|
| Related Catalog | |
| In Vitro | Lower concentrations of Fluensulfone delay development: 100 μM Fluensulfone causes a slight delay as at 66 h fewer worms have reached the adult stage whilst at 300 μM no worms reach the adult stage at 66 h and some fail to reach L4. Adult hermaphrodites lay fewer eggs in the presence of 1 mM Fluensulfone. Fluensulfone is also found to reduce the viability of eggs. After 3 h incubation with 100 μM to 1 mM Fluensulfone the thrashing rate is significantly inhibited, with maximal inhibition occurring with 1 mM. After 1 h both 300 μM and 1 mM Fluensulfone cause a significant and reversible inhibition of pharyngeal pumping relative to the vehicle control. Fluensulfone (500 μM) inhibits the frequency of body bends in one day old adult hermaphrodites off food after 2 h exposure[1]. |
| In Vivo | In an in vivo investigation, female mice are treated with Fluensulfone (or isoniazid as a positive control) for 3 and 7 days. Quantification of the cell proliferation by manual counting of BrdU-positive and BrdU-negative cells in the bronchiolar epithelium reveals an approximately fourfold increase of cell proliferation upon treatment with Fluensulfone and the positive control isoniazid compare with control. Increased cell proliferation is observed at 3 days but have reverted to the control level at day 7 [2]. |
| Cell Assay | For these assays worms of different developmental stages are incubated in liquid with and without Fluensulfone for up to 24 h, and paralysis is scored. 400 μL of M9 phosphate buffer with either Fluensulfone (100 μM, 200 μM or 1 mM) or vehicle (0.5% acetone) is put into each well of a 24 well plate (5 replicates for each Fluensulfone concentration). 5 μL suspension of age synchronised C. elegans (L1, L2/3, L4 or one day old adult) is added to each well. Each well contains approximately 50 to100 worms. The number of worms not moving at 1, 2, 3, 4, 5, 6 and 24 h is determined. The experiment is conducted on two separate occasions with five replicates[1]. |
| Animal Admin | Groups of 10 female specific pathogen-free CD-1 mice each are treated with untreated diet, diet containing 1200 mg/kg Fluensulfone (high dose in carcinogenicity study), or 1305 mg/kg of isoniazid as a positive control substance for 3 or 7 days, respectively. Two and 14 h before sacrifice, the animals are injected ip with 100 μL of a 10 mg/mL aqueous bromodeoxyuridine (BrdU)-solution. Sacrifice by exsanguination under deep irreversible pentobarbital narcosis is performed early in the morning to assure that the animals are exposed to the test item until shortly before sacrifice[2]. |
| References |
| Density | 1.6±0.1 g/cm3 |
|---|---|
| Boiling Point | 375.5±52.0 °C at 760 mmHg |
| Molecular Formula | C7H5ClF3NO2S2 |
| Molecular Weight | 291.698 |
| Flash Point | 180.9±30.7 °C |
| Exact Mass | 290.940216 |
| PSA | 83.65000 |
| LogP | 3.34 |
| Appearance of Characters | light yellow oil |
| Vapour Pressure | 0.0±0.8 mmHg at 25°C |
| Index of Refraction | 1.503 |
| Storage condition | -20℃ |
| 5-chloro-2-(3,4,4-trifluorobut-3-en-1-ylsulfonyl)-1,3-thiazole |
| Thiazole, 5-chloro-2-[(3,4,4-trifluoro-3-buten-1-yl)sulfonyl]- |
| 5-Chloro-2-[(3,4,4-trifluorobut-3-en-1-yl)sulfonyl]-1,3-thiazole |
| 5-Chloro-1,3-thiazol-2-yl 3,4,4-trifluorobut-3-en-1-yl sulfone |
| 11323358 |
| 5-Chloro-2-[(3,4,4-trifluoro-3-buten-1-yl)sulfonyl]thiazole |
| fluensulfone |
| T5N CSJ BSW2YFUYFF DG |
| 5-chloro-2-(3,4,4-trifluorobut-3-enylsulfonyl)-1,3-thiazole |
| 5-chloro-2-(3,4,4-trifluorobut-3-ene-1-sulfonyl)-1,3-thiazole |
| 5-Chloro-2-[(3,4,4-trifluoro-3-buten-1-yl)sulfonyl]-1,3-thiazole |