CAS No.75-02-5,VINYL FLUORIDE Suppliers

Dayang Chem (Hangzhou) Co.,Ltd.

As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch

Vinyl fluoride

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Ality Chemical Corporation

The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi

Factory Supply Fluoroethylene

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Chemwill Asia Co., Ltd.

Our main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block

Vinyl fluoride

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Zibo Hangyu Biotechnology Development Co., Ltd

Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi

Vinyl fluoride

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Min.Order:10 Gram

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DB BIOTECH CO., LTD

Q1: Are you a manufacturer Answer: Yes, we are factory founded on 2012.Q2: How to contact with us Click "contact supplier" And then send us message the product you interest in, you will get reply within 12 hours.Q3:Which kind of payment terms do you

VINYL FLUORIDE

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Henan Tianfu Chemical Co., Ltd.

1.Our services：A.Supply sampleB.The packing also can be according the customers` requirmentC.Any inquiries will be replied within 24 hoursD.we provide Commerical Invoice, Packing List, Bill of loading, COA , Health certificate and Origin certificate.

Ethene, fluoro-

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Antimex Chemical Limied

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

Ethene, fluoro-

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Zhuozhou Wenxi import and Export Co., Ltd

Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard

Hot selling products CAS 75-02-5 with fast delivery

Cas:75-02-5

Min.Order:1 Kilogram

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Changchun Artel lmport and Export trade company

Supply top quality products with a reasonable price Application:api

75-02-5

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Shanghai united Scientific Co.,Ltd.

United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat

Ethene, fluoro-

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Nanjing Raymon Biotech Co., Ltd.

fluoroethene Storage:Store in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/Pharmaceutical intermediates Transportation:By Sea,by Air,By courier like DHL or Fedx. Port:Shanghai/Shenzhen

fluoroethene

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Chemical Co.Ltd

Ethene, fluoro-Appearance:Off white to slight yellow solid Storage:Stored in shaded, cool and dry places Package:1L 5L 10L 25L bottle Application:pharma intermediate Transportation:Handle with cares to avoid damaging the packages. Protect them from s

Ethene, fluoro-

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NovaChemistry

high purity Application:Drug intermediates Materials intermediates and active molecules

fluoroethene

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Trans Intl Chem Shop

Vinyl fluoride

Cas:75-02-5

Min.Order:0 Metric Ton

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Engineered Controls International, Inc

Ethene, fluoro-

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Specialty Gases of America, Inc

Ethene, fluoro-

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Synthetic route

: 75-37-6
1,1-difluoroethane

: 74-86-2
acetylene

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
at 340℃; other temperatures, other catalysts;	77.5%

: 75-37-6
1,1-difluoroethane

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With hydrogen fluoride; Alpha-chromium oxide obtained from the pyrolysis of ammonium dichromate, treated with HF for 9 - 162h;	29.8%
With hydrogen fluoride; chromium(III) oxide at 245 - 275℃; for 5 - 49h; Catalys was activated in a stream of HF up to 350 C;	13.2%
With hydrogen fluoride; Alpha-chromium oxide obtained from the pyrolysis of ammonium dichromate, treated with HF at 200 - 245℃; for 15 - 47.5h;	6%

: 75-37-6
1,1-difluoroethane

A: 74-85-1
ethene

B: 75-02-5
1-fluoroethylene

C: 74-86-2
acetylene

Conditions

Conditions	Yield
With hydrogen fluoride; Guingnet's green at 250 - 400℃; for 10 - 129h;	A 0% B 19.6% C 0%
With hydrogen fluoride; Alpha-chromium oxide obtained from the pyrolysis of ammonium dichromate, treated with HF at 250 - 350℃;	A 0% B 19.3% C 0%
With hydrogen fluoride; Alpha-chromium oxide prepared by the precipitation of chromium hydroxide from chromium nitrate followed by calcination in air at 500 C for 72 hours, treated with HF at 250 - 350℃;	A 0% B 19.9% C 0%

...Expand

: 60-29-7
diethyl ether

: 598-39-0
1,1-difluoro-2-iodoethane

: phenylmagnesium bromide

A: 462-06-6
fluorobenzene

B: 591-50-4
iodobenzene

C: 92-52-4
biphenyl

D: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
Zersetzen des Reaktionsproduktes mit Wasser; Produkt5: Stilben;

...Expand

: 60-29-7
diethyl ether

: 358-97-4
1,2-bromofluoroethane

: phenylmagnesium bromide

A: 108-86-1
bromobenzene

B: 92-52-4
biphenyl

C: 75-02-5
1-fluoroethylene

D: 71-43-2
benzene

Conditions

Conditions	Yield
Zersetzen des Reaktionsproduktes mit Wasser;

...Expand

: 1615-75-4
1-chloro-1-fluoroethane

A: 75-02-5
1-fluoroethylene

B: 75-01-4
chloroethylene

Conditions

Conditions	Yield
at 600℃;

: 624-72-6
1,2-difluoroethane

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
at 103.9 - 201.9℃;
With calcium sulfate at 350℃;

: 359-07-9
2-bromo-1,1-difluoroethane

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With ethanol; zinc at 50℃;

: 598-39-0
1,1-difluoro-2-iodoethane

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With diethyl ether; phenylmagnesium bromide
With diethyl ether; magnesium
With diethyl ether; potassium
With diethyl ether; sodium

: 358-97-4
1,2-bromofluoroethane

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With ethanol; zinc
With diethyl ether; phenylmagnesium bromide
With potassium iodide

: 78-74-0
1,1,2-tribromoethane

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With bromine; antimony(III) fluoride at 100℃; und Behandeln des Reaktionsprodukts mit Zink in Aethanol;

: 74-86-2
acetylene

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With potassium cyanide; hydrogen fluoride; copper(l) cyanide; pyrographite at 160℃;
With hydrogen fluoride; mercury(II) oxide
With hydrogen fluoride; mercury(II) diacetate

: 17003-27-9
1-fluoro-1-nitro-ethane

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With (thermolysis) at 300 - 340℃; Kinetics;

: 593-60-2
Vinyl bromide

: 344-07-0
1-chloro-2,3,4,5,6-pentafluorobenzene

A: 75-02-5
1-fluoroethylene

B: 5488-71-1
tetrafluorobezyne

Conditions

Conditions	Yield
at 21.9℃; Irradiation;

...Expand

: 593-60-2
Vinyl bromide

A: 2366-31-6
(Z)-1-bromo-2-fluoroethylene

B: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With F at 0℃; under 112.5 Torr; Mechanism;

: 392-56-3
Hexafluorobenzene

: 74-85-1
ethene

A: 75-02-5
1-fluoroethylene

B: 653-34-9
2,3,4,5,6-pentafluorostyrene

C: 363-72-4
Pentafluorobenzene

D: 106-99-0
buta-1,3-diene

E: 74-86-2
acetylene

Conditions

Conditions	Yield
Mechanism; Irradiation;	A 8 % Chromat. B 24 % Chromat. C 12 % Chromat. D 7 % Chromat. E 19 % Chromat.

...Expand

: 187737-37-7
propene

A: 2229-07-4
methyl radical

B: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With fluorine under 0.8 Torr; Mechanism; Product distribution; Irradiation; study of the branching ratio and radical products under multi-photon ionization conditions; other reagents and products;

: 74-84-0
ethane

A: 2229-07-4
methyl radical

B: 2025-56-1
ethyl radical

C: 74-85-1
ethene

D: 75-02-5
1-fluoroethylene

E: 74-86-2
acetylene

Conditions

Conditions	Yield
With fluorine photoelectron spectrum of the product mixture; the ethyl radical was investigated;

...Expand

: 74-85-1
ethene

: 344-07-0
1-chloro-2,3,4,5,6-pentafluorobenzene

A: 75-02-5
1-fluoroethylene

B: 5488-71-1
tetrafluorobezyne

Conditions

Conditions	Yield
at 21.9℃; Irradiation;

...Expand

: 74-85-1
ethene

: 13453-52-6
monofluorocarbene

A: 2465-56-7
methylene

B: 593-53-3
Methyl fluoride

C: 75-02-5
1-fluoroethylene

D: 406-33-7
1-fluoropropene

E: 74-86-2
acetylene

Conditions

Conditions	Yield
In gas Rate constant; Thermodynamic data; Ambient temperature; Irradiation; ΔH;

...Expand

: 74-85-1
ethene

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With F In gas at -100℃; under 1E-07 Torr; Mechanism; Thermodynamic data; other temperatures, other collision energies; potential energy barrier to F atom addition to C2H4;
With F at -71.15 - 24.85℃; Kinetics; Substitution;

: 74-85-1
ethene

A: 75-02-5
1-fluoroethylene

B: 28761-00-4
β-Fluoroethyl radical

Conditions

Conditions	Yield
With fluorine In gas at 1226.9 - 2226.9℃; Rate constant;

: 762-49-2
2-fluoroethyl bromide

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
Mechanism; Irradiation;
Decomposition; Photolysis;

: 75-01-4
chloroethylene

: 344-07-0
1-chloro-2,3,4,5,6-pentafluorobenzene

A: 75-02-5
1-fluoroethylene

B: 5488-71-1
tetrafluorobezyne

Conditions

Conditions	Yield
at 21.9℃; Irradiation;

...Expand

: 430-51-3
1-fluoro-2-propanone

A: 74-84-0
ethane

B: 74-85-1
ethene

C: 353-36-6
1-fluoroethane

D: 624-72-6
1,2-difluoroethane

E: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
at 26.9℃; under 840 Torr; Rate constant; Product distribution; Irradiation; bath gas: He; further bath gases; further pressure;

...Expand

: 453-14-5
1,3-difluoro-propan-2-one

A: 593-53-3
Methyl fluoride

B: 624-72-6
1,2-difluoroethane

C: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
at 101.9 - 202.9℃; under 2.3 - 7.5 Torr; Irradiation;

...Expand

: 79-35-6
1,1'-dichloro-2,2'-difluoroethene

A: 74-85-1
ethene

B: 75-02-5
1-fluoroethylene

C: 1691-13-0
1,2-difluoroethene

D: 74-86-2
acetylene

Conditions

Conditions	Yield
With monosilane under 5 Torr; Mechanism; Product distribution; Irradiation; wave length 944.2 cm-1, ratio SiH4/C2Cl2F2 = 9.0;

...Expand

: 79-35-6
1,1'-dichloro-2,2'-difluoroethene

A: 75-02-5
1-fluoroethylene

B: 74-86-2
acetylene

Conditions

Conditions	Yield
With monosilane under 5 Torr; Mechanism; Product distribution; Irradiation; wave length 1033.5 cm-1, ratio SiH4/C2Cl2F2 = 9.6;

: 462-26-0
2-fluoroethyl acetate

A: 74-85-1
ethene

B: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
In toluene at 610℃; Product distribution;

: 462-26-0
2-fluoroethyl acetate

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
at 430.2 - 450.1℃; Rate constant;

: 75-02-5
1-fluoroethylene

: 162291-59-0
RuH(C6H5)(CO)(P(C(CH3)3)2CH3)2

: 878750-74-4
RuF(C2H3)(CO)(P(C(CH3)3)2CH3)2

Conditions

Conditions	Yield
In benzene-d6 byproducts: C6H6; all manipulations under Ar atm.; soln. of Ru compd. reacted with C2H3F at 1 atm for 12 h at room temp.; detected by 31P(1H) NMR spectra;	99%
With methyldi-t-butylphosphine In Cyclohexane-d12 byproducts: C6H6; all manipulations under Ar atm.; soln. of Ru and P compds. reacted in NMR tube with C2H3F at 1 atm for 12 h at room temp.; detected by 31P(1H) NMR spectra;	99%

: 75-02-5
1-fluoroethylene

: 2154-71-4
bis-trifluoromethyl-aminooxyl

: 67329-58-2
C6H3F13N2O2

Conditions

Conditions	Yield
for 21h; Ambient temperature;	98%

: 75-02-5
1-fluoroethylene

: 2714-60-5
tetrakis(trifluoromethyl)diphosphine

: 34250-88-9
1,2-Bis-(bis-trifluoromethyl-phosphanyl)-1-fluoro-ethane

Conditions

Conditions	Yield
50°C (120 h);	96%
Irradiation (UV/VIS); 20°C (94 h);	59%
Irradiation;

: 75-02-5
1-fluoroethylene

: 1357616-33-1
[Ir2H(CO)2(μ-CO)(bis(diethylphosphino)methane)2][B(3,5-(CF3)2C6H3)4]

A: 1357616-35-3
[Ir2(H)(CO)3(μ-CCH2)(bis(diethylphosphino)methane)2][B(3,5-(CF3)2C6H3)4]

B: 1357616-37-5
[Ir2(H)2(CO)2(μ-H)(μ-CCHF)(bis(diethylphosphino)methane)2][B(3,5-(CF3)2C6H3)4]

Conditions

Conditions	Yield
In dichloromethane-d2 (Ar); using Schlenk techniques; charging of NMR tube with (Ir2(CO)3(H)(PEt2CH2PEt2)2)(B((CF3)2C6H3)4), addn. of CD2Cl2, addn. of CFHCH2 via a gastight syringe, vigorous mixing for 30 min; monitoring by NMR, transferring to Schlenk tube, removal of solvent under vac., redissolving in Et2O, addn. of pentane, pptn.; elem. anal.;	A 94% B n/a

...Expand

: 75-02-5
1-fluoroethylene

: 6141-72-6
perfluoro(2,4-dimethyl-3-oxa-2,4-diazapentane)

A: O-[2-(Bis-trifluoromethyl-amino)-1-fluoro-ethyl]-N,N-bis-trifluoromethyl-hydroxylamine

B: O-[2-(Bis-trifluoromethyl-amino)-2-fluoro-ethyl]-N,N-bis-trifluoromethyl-hydroxylamine

Conditions

Conditions	Yield
for 240h; Ambient temperature; in vacuo;	A 93% B 6%

...Expand

: 75-02-5
1-fluoroethylene

: 430-66-0
1,1,2-Trifluoroethan

Conditions

Conditions	Yield
With xenon difluoride; silicon tetrafluoride at 20℃; for 5h; Fluorination;	93%

: 75-02-5
1-fluoroethylene

: 431-94-7
N-chlorobistrifluoromethylamine

A: 35060-90-3
1-(bis(trifluoromethyl)-amino)-2-fluoro-2-chloro-ethane

B: 35060-87-8
1-bis(trifluoromethyl)-amino-2-fluoro-2-chloro-ethane

Conditions

Conditions	Yield
In gas Irradiation (UV/VIS); photolysis for 0.5 h;	A 5% B 91%
In neat (no solvent, gas phase) Irradiation (UV/VIS); photolysis for 0.5 h;	A 5% B 91%
at 25°C for 10 d in dark;	A 7% B 88%

...Expand

: 75-02-5
1-fluoroethylene

: 758-43-0
N-bromobis(trifluoromethyl)amine

A: 1-(bis(trifluoromethyl)-amino)-2-bromo-1-fluoro-ethane

B: 25237-12-1
1-bis(trifluoromethyl)-amino-2-bromo-2fluoro-ethane

Conditions

Conditions	Yield
Irradiation (UV/VIS); at 20°C for 16 h;	A 6% B 89%
Irradiation (UV/VIS); at 20°C for 16 h;	A 6% B 89%
for 16h; Ambient temperature;
at 20°C for 12 weeks in dark; ratio of (CF3)2NCH2CHFBr:(CF3)2NCHFCH2Br = 9:1;
at 20°C for 12 weeks in dark; ratio of (CF3)2NCH2CHFBr:(CF3)2NCHFCH2Br = 9:1;

...Expand

: 75-02-5
1-fluoroethylene

: 5764-87-4
N-Jod-bis(trifluormethyl)-amin

A: 35060-93-6
1-bis(trimethylfluoro)-amino-2-fluoro-2-iodo-ethane

B: 35060-88-9
1-(bis(trifluoromethyl)-amino)-2-iodo-1-fluoro-ethane

Conditions

Conditions	Yield
Irradiation (UV/VIS); at 20°C for 1 h; in quartz tube;	A 89% B 7%
	A 2% B 89%
Irradiation (UV/VIS); at 20°C for 1 h; in quartz tube;	A 89% B 7%

...Expand

: 75-02-5
1-fluoroethylene

: 460-96-8
bis(trifluoromethyl)phosphine

: 27393-67-5
2-Fluoroaethyl-bis(trifluoromethyl)phosphin

Conditions

Conditions	Yield
Irradiation (UV/VIS); time of irradiation:44 h;	88%
for 44h; Irradiation;

: 75-02-5
1-fluoroethylene

: 23153-22-2
1,1,1,3-tetrachloro-3-fluoropropane

Conditions

Conditions	Yield
With tetrachloromethane; iron(III) chloride; iron; triethyl phosphate at 120 - 127℃; under 3000.3 - 6750.68 Torr; Autoclave; Inert atmosphere;	86%

: 75-02-5
1-fluoroethylene

: 1357616-33-1
[Ir2H(CO)2(μ-CO)(bis(diethylphosphino)methane)2][B(3,5-(CF3)2C6H3)4]

: 1357616-37-5
[Ir2(H)2(CO)2(μ-H)(μ-CCHF)(bis(diethylphosphino)methane)2][B(3,5-(CF3)2C6H3)4]

Conditions

Conditions	Yield
With trimethylamine-N-oxide In dichloromethane (Ar); using Schlenk techniques; cooling of flask with soln. of (Ir2(CO)3(H)(PEt2CH2PEt2)2)B((CF3)2C6H3)4 in CH2Cl2 to -80°C, transferringof cooled CH2Cl2 soln. of Me3NO via cannula, addn. of CFHCH2, slow warm ing to room temp., stirring for 1 h; removal of solvent, monitoring by NMR;	83%

: 301224-40-8
Hoveyda-Grubbs catalyst second generation

: 75-02-5
1-fluoroethylene

: (RuCl2(CHF)(4,5-dihydro-1,3-dimesitylimidazol-2-ylidene))2

Conditions

Conditions	Yield
In toluene byproducts: CH2CHC6H4OCH(CH3)2; High Pressure; (N2); exposure of toluene soln. of ruthenium compd. to vinyl fluoride at5 psig, cooling to -4°C, stirring for 3 h; cooling to -35°C for 30 min, filtration, wasing with pentane, drying in vac. for 30 min, stirring with benzene for 5 min, drying in vac. for 5 h, elem. anal.;	81.3%