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Cas:52-68-6
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Cas:52-68-6
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inquiryProduct Name Chlorophos Chemical Name ((2,2,2-trichloro-1-hydroxyethyl)dimethylphosphonate) CAS No 52-68-6 Appearance White crystal powder Spec
T he company has advanced technology, as well as a large number of excellent R & D team, to provide customers from the grams to one hundred kilograms and tons of high-quality products, competitive prices and quality service Appearance:White or
Cas:52-68-6
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High purity CAS 52-68-6 Trichlorfon in stock Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED intermediates (Fluorene,Carbazo
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Min.Order:1 Gram
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Type:Lab/Research institutions
inquiryProduct Detail Minimum Order Qty. 10 Gram
Cas:52-68-6
Min.Order:20 Metric Ton
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inquiryChlorophos CAS: 52-68-6 Specification melting point 77-81 °c boiling point 100°c density 1.73 refractive index 1.3439 storage temp. 2-8°c water solubility slightly
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Cas:52-68-6
Min.Order:1 Gram
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Product name: Trichlorphon(CAS:52-68-6) CAS No.:52-68-6 Molecule Formula:C4H8Cl3O4P Molecule Weight:257.44 Purity: 97.0% Package: 25kg/drum Description:White crystalline powder Manufacture Standards:Enterprise Standard
Cas:52-68-6
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Cas:52-68-6
Min.Order:1 Kilogram
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inquiryTrichlorphon 97%TC Organic Phosphorus CAS. NO.52-68-6 Application:Trichlorphon 97%TC Organic Phosphorus CAS. NO.52-68-6
Cas:52-68-6
Min.Order:0
Negotiable
Type:Other
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Cas:52-68-6
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inquirylow price high qualityAppearance:solid or liquid Storage:sealed in cool and dry place Package:As customer require Application:Parpharmaceutical Transportation:by sea or by airplane Port:any port in China
Conditions | Yield |
---|---|
at 34℃; Rate constant; |
diazomethane
(2,2,2-trichloro-1-hydroxy-ethyl)-phosphonic acid monomethyl ester
trichlorfon
chloral hydrate
phosphorous acid trimethyl ester
A
Dichlorvos
B
trichlorfon
Conditions | Yield |
---|---|
In hexane for 1h; Product distribution; Mechanism; | |
In hexane for 1h; |
chloral hydrate
phosphorous acid trimethyl ester
A
Dichlorvos
B
trichlorfon
C
dichlorovinylmethyl phosphoric acid
Conditions | Yield |
---|---|
In hexane for 10h; Heating; |
Conditions | Yield |
---|---|
With aluminum oxide for 0.1h; microwave irradiation; | 74 % Spectr. |
Conditions | Yield |
---|---|
With aluminum oxide; potassium fluoride at 20℃; for 0.5h; | |
With aluminum oxide; potassium fluoride | |
With aluminum oxide; potassium fluoride | |
With aluminum oxide; potassium fluoride |
chloral hydrate
phosphorous acid trimethyl ester
A
methanol
B
trichlorfon
Conditions | Yield |
---|---|
Abramov reaction; |
trichlorfon
2-(3-chloro-4-fluorophenoxy)acetyl chloride
O,O-dimethyl 1-(3-chloro-4-fluorophenoxyacetoxy)-2,2,2-trichloroethylphosphonate
Conditions | Yield |
---|---|
With triethylamine In chloroform at 2 - 20℃; | 80% |
2,6-Pyridinedicarbonyl dichloride
trichlorfon
O,O-dimethyl-2,6-pyridinyldi(formyloxy-trichloromethyl-methylphosphonate)
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20 - 40℃; for 5h; | 73% |
trichlorfon
2-(2-chloro-4-fluorophenoxy)acetyl chloride
Conditions | Yield |
---|---|
With triethylamine In chloroform at 20℃; for 2h; | 72.5% |
trichlorfon
trifluoroacetic anhydride
A
C6H7Cl3F3O5P
B
trifluoroacetic acid
Conditions | Yield |
---|---|
In 1,2-dichloro-ethane at 40℃; for 2h; | A 72% B n/a |
trichlorfon
2,2,3,3-tetrafluoropropionic acid anhydride
A
2,2,3,3-tetrafluoropropanoic acid
B
C7H8Cl3F4O5P
Conditions | Yield |
---|---|
In 1,2-dichloro-ethane at 40℃; for 2h; | A n/a B 70% |
trichlorfon
heptafluorobutyric anhydride
A
heptafluorobutyric Acid
B
C8H7Cl3F7O5P
Conditions | Yield |
---|---|
In 1,2-dichloro-ethane at 40℃; for 2h; | A n/a B 68% |
2-[4-(trifluoromethyl)phenoxy]acetyl chloride
trichlorfon
Conditions | Yield |
---|---|
With triethylamine In chloroform at 20℃; for 2h; | 66.5% |
Conditions | Yield |
---|---|
With triethylamine In chloroform at 20℃; | 65.2% |
Conditions | Yield |
---|---|
With pyridine In chloroform at 10 - 42℃; | 62% |
(3,5-difluoro-phenoxy)-acetyl chloride
trichlorfon
Conditions | Yield |
---|---|
With triethylamine In chloroform at 20℃; | 59.7% |
trichlorfon
phosphorochloridic acid diisobutyl ester
(2,2,2-trichloro-1-diisobutoxyphosphoryloxy-ethyl)-phosphonic acid dimethyl ester
Conditions | Yield |
---|---|
With diethyl ether; diethylamine |
Conditions | Yield |
---|---|
With sodium hydroxide |
trichlorfon
propionyl chloride
(2,2,2-trichloro-1-propionyloxy-ethyl)-phosphonic acid dimethyl ester
Conditions | Yield |
---|---|
With diethyl ether; triethylamine |
trichlorfon
Diisopropyl chlorophosphate
(2,2,2-trichloro-1-diisopropoxyphosphoryloxy-ethyl)-phosphonic acid dimethyl ester
Conditions | Yield |
---|---|
With diethyl ether; diethylamine |
trichlorfon
dipropyl chlorophosphate
(2,2,2-trichloro-1-dipropoxyphosphoryloxy-ethyl)-phosphonic acid dimethyl ester
Conditions | Yield |
---|---|
With diethyl ether; diethylamine |
trichlorfon
acetyl chloride
(1-acetoxy-2,2,2-trichloro-ethyl)-phosphonic acid dimethyl ester
Conditions | Yield |
---|---|
With diethyl ether; triethylamine |
trichlorfon
isobutyryl chloride
(2,2,2-trichloro-1-isobutyryloxy-ethyl)-phosphonic acid dimethyl ester
Conditions | Yield |
---|---|
With diethyl ether; triethylamine |
trichlorfon
butyryl chloride
(1-butyryloxy-2,2,2-trichloro-ethyl)-phosphonic acid dimethyl ester
Conditions | Yield |
---|---|
With diethyl ether; triethylamine |
trichlorfon
Dimethyl chlorophosphate
(2,2,2-trichloro-1-diethoxyphosphoryloxy-ethyl)-phosphonic acid dimethyl ester
Conditions | Yield |
---|---|
With diethyl ether; diethylamine |
trichlorfon
Dimethyl chlorophosphate
(2,2,2-trichloro-1-dimethoxyphosphoryloxy-ethyl)-phosphonic acid dimethyl ester
Conditions | Yield |
---|---|
With diethyl ether; diethylamine |
trichlorfon
2-Bromopropionyl chloride
[1-(2-bromo-propionyloxy)-2,2,2-trichloro-ethyl]-phosphonic acid dimethyl ester
Conditions | Yield |
---|---|
With diethyl ether; triethylamine |
trichlorfon
dibutyl chlorophosphate
(2,2,2-trichloro-1-dibutoxyphosphoryloxy-ethyl)-phosphonic acid dimethyl ester
Conditions | Yield |
---|---|
With diethyl ether; diethylamine |
dichloroacethyl chloride
trichlorfon
<1-Dichloracetoxy-2.2.2-trichlor-aethyl>-phosphonsaeure-dimethylester
Conditions | Yield |
---|---|
With triethylamine In diethyl ether; benzene |
trichlorfon
diisopropyl phosphorisocyanatidate
O,O-Diisopropyl-phosphonocarbamidsaeure-<2,2,2-trichlor-1-(O,O-dimethyl-phosphono)-aethylester>
Conditions | Yield |
---|---|
In diethyl ether |
Conditions | Yield |
---|---|
(electrochemical reduction); |
Conditions | Yield |
---|---|
With sodium iodide In butanone Heating; |
trichlorfon
acryloyl chloride
Acrylic acid 2,2,2-trichloro-1-(dimethoxy-phosphoryl)-ethyl ester
Conditions | Yield |
---|---|
With sodium carbonate; hydroquinone In benzene |
trichlorfon
ethyl isocyanate
O,O-Dimethyl-2,2,2-trichlor-1-(N-ethyl)-carbamoylethyl-phosphonat
Conditions | Yield |
---|---|
With triethylamine In benzene Heating; |
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