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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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inquirysuperior quality moderate price & quick delivery Appearance:gas Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Used for Pesticide intermediat
Cas:372-64-5
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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
Cas:372-64-5
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
Cas:372-64-5
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inquiryZhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed
Cas:372-64-5
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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
high qualityAppearance:white crystalline powder Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
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inquiry1. Product advantages? High purity, all above 98.5%, no impurities after dissolution? We will test each batch to ensure quality? OEM and private brand services designed for free? Various cap colors available? We can also provide MT1 peptide powder2.
Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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inquiryBIS(TRIFLUOROMETHYL)DISULFIDEAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:pharmaceutical intermediate Transportation:by air, by sea, by express
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Cas:372-64-5
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China
Cas:372-64-5
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China
Cas:372-64-5
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inquiryfactory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Bis(trifluoromethyl) disulfide Application:2025690
Cas:372-64-5
Min.Order:1 Gram
FOB Price: $500.0
Type:Trading Company
inquiry*stable huge quantity supply*best service*powerful r&d team*gmp standard factory*we have the separate r&d dept.,the advanced equipments and the experienced engineers,we have established the excellent cooperative relations with many famous universitie
Our company provides the best service for our customers. Under the premise of ensuring quality and delivery date, give customers the best price. The company is more willing to meet our customers. If you want to visit our factories and warehouses, we
high purity Application:Drug intermediates Materials intermediates and active molecules
Cas:372-64-5
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inquirymercury bis(trifluoromethanethiolate)
A
Bis(trifluoromethyl)disulfid
C
bis(trifluoromethylthio)tellurium
Conditions | Yield |
---|---|
With tellurium tetrachloride for 1h; Heating; | A n/a B n/a C 83% |
Conditions | Yield |
---|---|
390-420°C, atm. pessure in a continuous flow system; | 80.6% |
390-420°C, atm. pessure in a continuous flow system; | 80.6% |
>200°C, in autoclave; | |
>200°C, in autoclave; |
O,O-diethyl S-trifluoromethyl phosphorothioate
A
thiocarbonyl fluoride
B
diethyl fluorophosphate
C
Bis(trifluoromethyl)disulfid
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 10℃; for 0.166667h; | A n/a B 76% C n/a |
mercury bis(trifluoromethanethiolate)
dimethylamino sulfonyl chloride
A
Bis(trifluoromethyl)disulfid
Conditions | Yield |
---|---|
In acetonitrile | A n/a B 76% |
hydrogen fluoride
chlorothio-trichloro-methane
A
Trifluoromethylsulfenyl chloride
B
Bis(trifluoromethyl)disulfid
C
Trifluoro-methanethiosulfonic acid S-trifluoromethyl ester
Conditions | Yield |
---|---|
180°C; chrom oxide fluoride catalyst; | A 74% B n/a C n/a |
dimethyl(bromo)arsine
Copper(I) trifluoromethanethiolate
A
Bis(trifluoromethyl)disulfid
B
bis(trifluoromethyl)trisulfide
C
bis(trifluoromethyl)tetrasulfide
D
dimethyl(trifluoromethylthio)arsine
Conditions | Yield |
---|---|
at 80 - 90℃; for 6h; Further byproducts given; | A n/a B n/a C n/a D 70% |
Trifluoromethylsulfenyl chloride
toluene
A
Bis(trifluoromethyl)disulfid
B
benzyl trifluoromethyl sulfide
C
benzyl chloride
Conditions | Yield |
---|---|
byproducts: HCl; Irradiation (UV/VIS); | A n/a B 70% C 3% |
byproducts: HCl; Irradiation (UV/VIS); | A n/a B 70% C 3% |
for 0.283333h; Mechanism; Irradiation; effect of bis(heptafluoro-n-propyl) disulfide; |
Conditions | Yield |
---|---|
With hydrogen bromide In further solvent(s) 160-175°C; solvent: tetramethylenesulfone; | 68% |
With HBr In further solvent(s) 160-175°C; solvent: tetramethylenesulfone; | 68% |
Conditions | Yield |
---|---|
In further solvent(s) 150-160°C; solvent: tetramethylenesulfone; | 58% |
In further solvent(s) 150-160°C; solvent: tetramethylenesulfone; | 58% |
2-phenyl-1H-pyrrole
1-phenyl-2-(phenyl-λ3-iodaneylidene)-2-((trifluoromethyl)sulfonyl)ethan-1-one
A
Bis(trifluoromethyl)disulfid
Conditions | Yield |
---|---|
Stage #1: 1-phenyl-2-(phenyl-λ3-iodaneylidene)-2-((trifluoromethyl)sulfonyl)ethan-1-one With copper (II)-fluoride In 1-methyl-pyrrolidin-2-one at 20℃; for 0.333333h; Stage #2: 2-phenyl-1H-pyrrole at 20℃; for 5h; regioselective reaction; | A 28% B 58% |
Trifluoromethylsulfenyl chloride
sodium acetate
A
Bis(trifluoromethyl)disulfid
B
Trifluoro-methanethiosulfonic acid S-trifluoromethyl ester
C
trifluoromethyl-sulfenyl acetate
D
acetic anhydride
Conditions | Yield |
---|---|
at 0℃; for 12h; | A n/a B n/a C 52% D n/a |
tris(trifluoromethylmercapto)amine
A
Bis(trifluoromethyl)disulfid
B
tetrakis (trifluormethylmarcapto)-hydrazine
Conditions | Yield |
---|---|
In trichlorofluoromethane at -73.1℃; for 6h; Irradiation; | A n/a B 50% |
In trichlorofluoromethane at -73.1℃; for 6h; Product distribution; Irradiation; other temperature 298 deg K; | A n/a B 10 % Turnov. |
methyldichloroarsane
mercury bis(trifluoromethanethiolate)
A
methyldifluoroarsine
B
Bis(trifluoromethyl)disulfid
C
bis(trifluoromethyl)trithiocarbonate
Conditions | Yield |
---|---|
at 95 - 100℃; for 4h; | A n/a B n/a C n/a D 48% |
Trifluoromethylsulfenyl chloride
Isobutane
B
tertiary butyl chloride
C
2-methyl-2-[(trifluoromethyl)thio]propane
D
Bis(trifluoromethyl)disulfid
E
isobutyryl chloride
Conditions | Yield |
---|---|
byproducts: HCl; Irradiation (UV/VIS); | A 12% B 33% C 24% D 47% E 1% |
byproducts: HCl; Irradiation (UV/VIS); | A 12% B 33% C 24% D 47% E 1% |
Trifluoromethylsulfenyl chloride
n-butane
A
s-butyl chloride
B
n-Butyl chloride
C
Bis(trifluoromethyl)disulfid
D
Trifluormethyl-sek.-butyl-sulfid
E
1-[(trifluoromethyl)thio]butane
Conditions | Yield |
---|---|
byproducts: HCl; Irradiation (UV/VIS); | A 12% B 1% C 28% D 46% E 13% |
byproducts: HCl; Irradiation (UV/VIS); | A 12% B 1% C 28% D 46% E 13% |
Trifluoromethylsulfenyl chloride
cyclohexane
A
Bis(trifluoromethyl)disulfid
B
cyclohexyl(trifluoromethyl)sulfane
C
cyclohexyl chloride
Conditions | Yield |
---|---|
byproducts: HCl; Irradiation (UV/VIS); | A 35% B 45% C 28% |
byproducts: HCl; Irradiation (UV/VIS); | A 35% B 45% C 28% |
for 0.2h; Mechanism; Irradiation; effect of bis(heptafluoro-n-propyl) disulfide; |
Trifluoromethylsulfenyl chloride
dihydrogen peroxide
A
Bis(trifluoromethyl)disulfid
B
trifluorormethanesulfonic acid
C
trifluoromethane sulfonyl chloride
Conditions | Yield |
---|---|
35% H2O2 soln.; | A 35% B 7% C 40% |
35% H2O2 soln.; | A 35% B 7% C 40% |
Trifluoromethylsulfenyl chloride
A
Bis(trifluoromethyl)disulfid
B
tetrakis(trifluoromethylthiazyl)
Conditions | Yield |
---|---|
With trimethylsilylazide In trichlorofluoromethane at -30℃; for 24h; | A n/a B 37% |
furan
Trifluoromethylsulfenyl chloride
A
2-Trifluormethylmercapto-furan
B
Bis(trifluoromethyl)disulfid
Conditions | Yield |
---|---|
With pyridine at 20℃; for 12h; other sulfenyl chloride; | A 35% B n/a |
With pyridine at 20℃; for 12h; | A 35% B n/a |
Conditions | Yield |
---|---|
-183 to 25°C; | 30% |
-183 to 25°C; | 30% |
bis(fluorosulfuryl) peroxide
trifluoromethylsulfide
A
fluorosulfonyl anhydride
B
Bis(trifluoromethyl)disulfid
C
sulfur dioxide
D
sulfur
Conditions | Yield |
---|---|
CF3SH:S2O6F2 molar ratio 1:1, from -183 to +25°C; | A n/a B 30% C n/a D n/a |
ethylarsenic dichloride
Copper(I) trifluoromethanethiolate
A
Bis(trifluoromethyl)disulfid
B
trifluoromethylmercaptothiocarbonyl fluoride
C
bis(trifluoromethyl)trisulfide
Conditions | Yield |
---|---|
at 85 - 95℃; for 6h; Further byproducts given; | A n/a B n/a C n/a D 25% |
Conditions | Yield |
---|---|
Irradiation (UV/VIS); in Pyrex bulb; | A n/a B 25% |
Irradiation (UV/VIS); in Pyrex bulb; | A n/a B 25% |
Conditions | Yield |
---|---|
With sulfolane; potassium fluoride at 175℃; Inert atmosphere; | 15% |
Trifluoromethylsulfenyl chloride
A
Bis(trifluoromethyl)disulfid
B
hexachloro-3-cyclopentenylidenaminotrifluormethylsulfide
Conditions | Yield |
---|---|
With trimethylsilylazide; hexachlorocyclopentadiene In toluene at 110℃; under 0.01 Torr; for 3h; | A n/a B 6.2% |
Trifluoromethylsulfenyl chloride
trimethylsilylazide
hexachlorocyclopentadiene
A
Bis(trifluoromethyl)disulfid
B
hexachloro-3-cyclopentenylidenaminotrifluormethylsulfide
Conditions | Yield |
---|---|
In toluene at 110℃; under 0.01 Torr; for 3h; | A n/a B 6.2% |
Conditions | Yield |
---|---|
With iodine pentafluoride at 195℃; | |
With mercury(II) fluoride at 500℃; |
Conditions | Yield |
---|---|
With sulfur at 310℃; |
Conditions | Yield |
---|---|
With sulfur tetrafluoride at 250℃; |
Conditions | Yield |
---|---|
iron pentacarbonyl In tetrahydrofuran at -80℃; | |
With perfluoropropylene for 72h; Irradiation; | |
With trifluoro-methoxy-ethene for 0.166667h; Irradiation; Further byproducts given; |
propene
Bis(trifluoromethyl)disulfid
1,2-Bis-trifluoromethylsulfanyl-propane
Conditions | Yield |
---|---|
Irradiation (UV/VIS); 20 h; | 100% |
Irradiation (UV/VIS); 20 h; | 100% |
Irradiation; |
Conditions | Yield |
---|---|
Irradiation (UV/VIS); 44 h; | 100% |
Irradiation (UV/VIS); 44 h; | 100% |
Irradiation; |
Conditions | Yield |
---|---|
In 1,2-dimethoxyethane at -20℃; for 0.166667h; Reduction; | 98.3% |
Bis(trifluoromethyl)disulfid
benzyl tetraethylphosphorodiamidite
A
benzyl trifluoromethyl sulfide
Conditions | Yield |
---|---|
In pentane at -50℃; for 0.0833333h; | A 95% B n/a |
chlorine trifluoride
Bis(trifluoromethyl)disulfid
trifluoro(trifluoromethyl)sulfur(IV)
Conditions | Yield |
---|---|
In dichloromethane -78°C; | 95% |
In dichloromethane -78°C; | 95% |
In Dichlorodifluoromethane excess ClF3, -196 to -78°C; | |
In Dichlorodifluoromethane excess ClF3, -196 to -78°C; |
perfluoropropylene
Bis(trifluoromethyl)disulfid
A
2,5-bis(trifluoromethylmercapto)-4-trifluoromethyl-nonafluoropentane
B
1,2-bis(trifluoromethylsulfanyl)hexafluoropropane
Conditions | Yield |
---|---|
Irradiation (UV/VIS); 184 h; | A 90.5% B 9.5% |
Irradiation (UV/VIS); 184 h; | A 90.5% B 9.5% |
Bis(trifluoromethyl)disulfid
A
Ethyl <(trifluoromethyl)thio>acetate
Conditions | Yield |
---|---|
In pentane at -50℃; for 0.0833333h; | A 90% B n/a |
Bis(trifluoromethyl)disulfid
A
Ethyl 2-<(trifluoromethyl)thio>propanoate
Conditions | Yield |
---|---|
In pentane at -50℃; for 0.0833333h; | A 90% B n/a |
Bis(trifluoromethyl)disulfid
Tetrakis(trifluoromethyl)cyclotetraphosphane
A
Trifluormethyl-(bis-methylmercapto)-phosphin
B
pentakis-trifluoromethyl-cyclopentaphosphane
Conditions | Yield |
---|---|
143°C, 1 h; | A 90% B n/a |
143°C, 1 h; | A 90% B n/a |
20°C, 12 h; | |
20°C, 12 h; |
tetrakis(triphenylphosphine) palladium(0)
Bis(trifluoromethyl)disulfid
Pd(SCF3)2{P(C6H5)3}2
Pd(SCF3)2{P(C6H5)3}2
Conditions | Yield |
---|---|
In pentane Irradiation (UV/VIS); with low-pressure mercury lamp, 25°C, 30 min; | A 10% B 90% |
In pentane Irradiation (UV/VIS); with low-pressure mercury lamp, 25°C, 30 min; | A 10% B 90% |
Bis(trifluoromethyl)disulfid
fluorine
trifluoro(trifluoromethyl)sulfur(IV)
Conditions | Yield |
---|---|
fluorination with F2/He (flow rate 1 mL/min F2 and 60 mL min He) in continuous flow reactor at -120°C (38 h); | 90% |
fluorination with F2/He (flow rate 1 mL/min F2 and 60 mL min He) in continuous flow reactor at -120°C (38 h); | 90% |
with N2 dild. F2 used; | |
with N2 dild. F2 used; |
Conditions | Yield |
---|---|
In pentane Irradiation (UV/VIS); medium-pressure mercury lamp, 25 h; | 90% |
In pentane Irradiation (UV/VIS); medium-pressure mercury lamp, 25 h; | 90% |
dimanganese decacarbonyl
Bis(trifluoromethyl)disulfid
A
Mn2(CO)8(SCF3)2
B
CF3SMn(CO)5
Conditions | Yield |
---|---|
In pentane Irradiation (UV/VIS); medium-pressure mercury lamp, -10°C, 24 h; | A 90% B n/a |
In pentane Irradiation (UV/VIS); medium-pressure mercury lamp, -10°C, 24 h; | A 90% B n/a |
Conditions | Yield |
---|---|
heating at 425-435°C, 3-4 d; | 88% |
Irradiation (UV/VIS); in quartztube, 13 d; | 39% |
Irradiation (UV/VIS); in quartztube, 13 d; | 39% |
Irradiation.UV-Licht; |
Bis(trifluoromethyl)disulfid
(Rp)-t-butyl(phenyl)phosphine oxide
(-)-S-t-butyl(phenyl)-S-trifluoromethyl phosphinothioate
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 6h; | 88% |
hydrido(tricarbonyl)(cyclopentadienyl)molybdenum
Bis(trifluoromethyl)disulfid
Conditions | Yield |
---|---|
In benzene byproducts: HSCF3; (N2 or in vacuum with Schlenk-technique); react. at 25°C for 2 d; chromy. on SiO2-column with benzene/cyclohexane; | 87.3% |
Bis(trifluoromethyl)disulfid
tert-Butylphenylphosphine oxide
Conditions | Yield |
---|---|
In dichloromethane -85 to -80 deg C, 30 min, then 15-20 deg C, 5 h; | 85% |
Bis(trifluoromethyl)disulfid
2-diethylamino-1,3,2-dioxaphosphorinane
Conditions | Yield |
---|---|
In dichloromethane -85 to -80 deg C, 30 min, then 15-20 deg C, 5 h; | 85% |
Bis(trifluoromethyl)disulfid
Conditions | Yield |
---|---|
With cesium fluoride In 1,2-dimethoxyethane at 85℃; for 24h; Inert atmosphere; Sealed tube; | 84% |
Conditions | Yield |
---|---|
In dichloromethane -85 to -80 deg C, 30 min, then 15-20 deg C, 5 h; | 83% |
Conditions | Yield |
---|---|
With cesium fluoride In 1,2-dimethoxyethane at 110℃; for 48h; Inert atmosphere; Sealed tube; | 83% |
Bis(trifluoromethyl)disulfid
Conditions | Yield |
---|---|
With cesium fluoride In 1,2-dimethoxyethane at 110℃; for 37h; Inert atmosphere; Sealed tube; | A n/a B 82% |
Conditions | Yield |
---|---|
In dichloromethane -85 to -80 deg C, 30 min, then 15-20 deg C, 5 h; | 81% |
Bis(trifluoromethyl)disulfid
4-methoxy-N-(8-quinolinyl)benzamide
N-(2,6-di(trifluoromethylthio)-4-methoxybenzoyl)-8-aminoquinoline
Conditions | Yield |
---|---|
With copper diacetate In dimethyl sulfoxide at 100℃; for 5.75h; | 81% |
Bis(trifluoromethyl)disulfid
4-methoxy-aniline
4-methoxyphenyl trifluoromethylsulfide
Conditions | Yield |
---|---|
Stage #1: 4-methoxy-aniline With tetrafluoroboric acid; tert.-butylnitrite In water; acetic acid at 20℃; for 0.0833333h; Green chemistry; Stage #2: Bis(trifluoromethyl)disulfid With sodium acetate In dimethyl sulfoxide at 20℃; for 8h; Inert atmosphere; Green chemistry; | 81% |
Stage #1: 4-methoxy-aniline With tetrafluoroboric acid; sodium nitrite In water at 0℃; for 0.666667h; Stage #2: Bis(trifluoromethyl)disulfid With tris(bipyridine)ruthenium(II) dichloride hexahydrate In dimethyl sulfoxide at 20℃; for 1h; Reagent/catalyst; Inert atmosphere; Irradiation; | 131.2 mg |
Bis(trifluoromethyl)disulfid
Conditions | Yield |
---|---|
With cesium fluoride In 1,2-dimethoxyethane at 110℃; for 46h; Inert atmosphere; Sealed tube; | 81% |
Bis(trifluoromethyl)disulfid
phosphorous acid trimethyl ester
A
methyl trifluoromethyl sulphide
B
O,O-dimethyl-S-trifluoromethyl phosphorthioate
Conditions | Yield |
---|---|
In dichloromethane 1) -75 deg C, 2) 20 deg C, 50 min; | A n/a B 80% |
In dichloromethane -75 to 20°C; | A n/a B 80% |
In dichloromethane -75 to 20°C; | A n/a B 80% |
Bis(trifluoromethyl)disulfid
Conditions | Yield |
---|---|
In dichloromethane a soln. of Mo-complex and CF3SSCF3 was stirred under N2 at room temp. for 2 h (IR monitoring); solvent was removed by evapn. under a stream of N2, product purified by chromy. on Al2O3 and crystn.; | 80% |
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