FLUORODIFEN
- Product Name
- FLUORODIFEN
- CAS No.
- 15457-05-3
- Chemical Name
- FLUORODIFEN
- Synonyms
- Soyex;C 6989;C 6929;Preferan;Preforan;NSC 58415;Flurodifen;Fluordifen;FLUORODIFEN;PREFORAN(R)
- CBNumber
- CB4754044
- Molecular Formula
- C13H7F3N2O5
- Formula Weight
- 328.2
- MOL File
- 15457-05-3.mol
FLUORODIFEN Property
- Melting point:
- 94℃
- Boiling point:
- 371.1±42.0 °C(Predicted)
- Density
- 1.5601 (estimate)
- solubility
- Chloroform (Slightly), Methanol (Slightly)
- color
- Yellowish-brown crystals
- Water Solubility
- 2mg/L(20 ºC)
- BRN
- 2018474
- EPA Substance Registry System
- Fluorodifen (15457-05-3)
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H319Causes serious eye irritation
H332Harmful if inhaled
H400Very toxic to aquatic life
- Precautionary statements
-
P273Avoid release to the environment.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- 45506
- Product name
- Fluorodifen
- Purity
- PESTANAL
- Packaging
- 250mg
- Price
- $15.96
- Updated
- 2024/03/01
- Product number
- F590968
- Product name
- Fluorodifen
- Packaging
- 10mg
- Price
- $40
- Updated
- 2021/12/16
- Product number
- F590968
- Product name
- Fluorodifen
- Packaging
- 25mg
- Price
- $90
- Updated
- 2021/12/16
- Product number
- 450204
- Product name
- Fluorodifen
- Packaging
- 10mg
- Price
- $305
- Updated
- 2021/12/16
FLUORODIFEN Chemical Properties,Usage,Production
Definition
ChEBI: Fluorodifen is an aromatic ether.
Safety Profile
Mildly toxic by ingestion. An eyeirritant. Used as an herbicide. When heated todecomposition it emits very toxic fumes of NOx and Fí.
Metabolic pathway
Photopysis products of eight substituted diphenyl ethers (preforan, nitrofen, MC-338, MC-4379, MC-3761, MC-5127, MC-6063, and MC-7181) irradiated by a Raryonette reactor in solutions of water, cyclohexane, and methanol indicates that the major reaction pathways of these biphenyl ethers include reductive dehalogenation, decarboxyalkylation, reduction of nitro substituents to amines, and cleavage of the ether linkage to yield phenols.
FLUORODIFEN Preparation Products And Raw materials
Raw materials
Preparation Products
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