Acifluorfen
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Acifluorfen
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CAS No:
50594-66-6
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Formula:
C14H7ClF3NO5
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Chemical Name:
Acifluorfen
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Synonyms:
Benzoic acid,5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitro-;5-[2-Chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoic acid;Acifluorfen;2-Nitro-5-(2-chloro-4-trifluoromethylphenoxy)benzoic acid;3-Carboxy-2′-chloro-4′-trifluoromethyl-4-nitrodiphenyl ether;PPG 847;Acifluorfene;Acifluorfen H;94128-04-8
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CAS No:
Description
A diphenyl ether, is a combustible, off-white, light tan or brown solid.
Solid
Acifluorfen is a member of the class of benzoic acids that is 2-nitrobenzoic acid in which the hydrogen at position 5 is replaced by a 2-chloro-4-(trifluoromethyl)phenoxy group. It is a herbicide used for the post-emergence control of a variety of annual broadleaf weeds. It has a role as a herbicide, an agrochemical and an EC 1.3.3.4 (protoporphyrinogen oxidase) inhibitor. It is a member of benzoic acids, an organochlorine compound, an organofluorine compound, an aromatic ether, a monocarboxylic acid and a C-nitro compound.|Acifluorfen is a protoporphyrinogen oxidase inhibitor.
Characteristics
92.4
3.70
Solid
1.26 at 23 deg C
150 °C
>100 deg C /47% WATER SOLUTION/
209.2±28.7 °C
1.576
>54.2 [ug/mL]
0-6°C
<1.3X10-3 mPa.
Safety Information
III
UN 3077
3
22-38-41-50/53
24-39-60-61
DG5643070
Xn;N,N,Xn
Stable in acid and alkaline media, pH 3 to pH 9 (40 deg C). /Acifluorfen/
P273-P280-P305 + P351 + P338-P501
H302-H315-H318-H410
|Danger|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P273, P280, P301+P312, P302+P352, P305+P351+P338, P310, P321, P330, P332+P313, P362, P391, and P501|Aggregated GHS information provided by 163 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|H302: Harmful if swallowed [Warning Acute toxicity, oral]
Drug Information
Compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction. (See all compounds classified as Enzyme Inhibitors.)|Pesticides used to destroy unwanted vegetation, especially various types of weeds, grasses (POACEAE), and woody plants. Some plants develop HERBICIDE RESISTANCE. (See all compounds classified as Herbicides.)
5-(2-chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoate
Acifluorfen Use and Manufacturing
Using meta-hydroxybenzoic acid as raw material, equimolar 3, 4-dichlorobenzotrifluoride and meta-hydroxybenzoic acid are reacted at 138~144℃ for 22h in the presence of KOH with dimethyl sulfoxide as solvent to produce 3 -(2-Chloro-4-trifluoromethylphenoxy)benzoic acid. Then in the methylene chloride solvent, potassium nitrate-sulfuric acid is used for nitration reaction to generate acifluorfen. Then react with equimolar NaOH to form sodium salt. Using m-cresol as raw material, equimolar 3, 4-dichlorobenzotrifluoride and m-cresol potassium salt are reacted in a solvent at 149~155℃ to produce 3-(2-chloro-4-trifluoromethyl) Benzene is then oxidized in the presence of a catalyst and acetic acid with air at 94~96℃ to obtain 3-(2-chloro-2-trifluoromethylphenoxy)benzoic acid. The mixed acid is nitrated at 45°C in the presence of solvent and vinegar rod to obtain acifluorfen, and then reacted with equimolar NaOH to form sodium salt. Using 3-chloro-4-hydroxybenzotrifluoride as a raw material, equimolar 3-chloro-4-hydroxybenzotrifluoride and 5-chloro-2-nitrobenzoic acid in the solvent DMSO, potassium carbonate and nitrogen protection, in Reaction at room temperature to generate acifluorfen.
It is a contact herbicide. It is used for early post-emergence treatment and can be absorbed by weeds, stems, and leaves.
Benzoic acid, 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitro-: ACTIVE
Agrochemicals -> Herbicides
Computed Properties
Molecular Weight:361.65
XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:3
Exact Mass:360.9964845
Monoisotopic Mass:360.9964845
Topological Polar Surface Area:92.4
Heavy Atom Count:24
Complexity:484
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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Diquat dichloride Formula
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2,4-DB dimethylammonium Formula
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Fenchlorazole-ethyl Structure
103112-35-2
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