DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:355-43-1
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inquiryhebei yanxi chemical co., LTD who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do research and developm
Cas:355-43-1
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inquiryExcellent manufacturer supply Perfluoro-1-iodohexane CAS 355-43-1 with good quality Company profile Wuhan Fortuna Chemical Co.,Ltd established in 2006, is a big integrative chemical enterprise being engaged in Pharmaceutical & its intermedia
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inquiryhigh quality Appearance:Colorless liquid Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai
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
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Cas:355-43-1
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inquiryProduct Name: Perfluoro-1-iodohexane Synonyms: 1-IODOPERFLUOROHEXANE , STABILIZED WITH COPPER;1-IODOPERFLUOROHEXANE, 98+%, STAB. WITH COPPER;1-Iodoperfluorohexane, 1-Iodotridecafluorohexane, Tridecafluorohexyl iodide;1-Iodoperfluorohex
Cas:355-43-1
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inquiryOur advantages: 1. All inquiries will be replied within 12 hours. 2. Dedication to quality, supply & service. 3. Strictly on selecting raw materials. 4. Reasonable & competitive price, fast lead time. 5. Sample is available for your eva
Cas:355-43-1
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
Cas:355-43-1
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inquiryChemical Name: Perfluoro-1-iodohexane CAS No.:355-43-1 Molecular Fomula: C6F13I Chemical Structure: Molecular weight: 445.95 Appearance:Light pink liquid Appearance:Light pink liquid Storage:Store in cool and dry place, away from sun l
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Cas:355-43-1
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inquiryProduct Name: Perfluoro-1-iodohexane Synonyms: 1-IODOPERFLUOROHEXANE , STABILIZED WITH COPPER;1-IODOPERFLUOROHEXANE, 98+%, STAB. WITH COPPER;1-Iodoperfluorohexane, 1-Iodotridecafluorohexane, Tridecafluorohexyl iodide;1-Iodoperfluorohexane, 1-Io
Cas:355-43-1
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inquiryPerfluoro-1-iodohexane CAS:355-43-1 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic int
Cas:355-43-1
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
Cas:355-43-1
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Cas:355-43-1
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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
Perfluoro-1-iodohexane CAS:355-43-1 Specification Item Specification Appearance Clear Colorless Liquid Assay 98%min Density 2.063 g/mL at 25 °C(lit.) Boiling Point 117 °C(lit.)
Cas:355-43-1
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inquiryHangzhou Fanda Chemical Co.,Ltd (FandaChem) , a China-based chemical company, specialize in exporting Perfluoro-1-iodohexane CAS:355-43-1, Please contact us by email freely. We are leading exporter in China. If you really need
Cas:355-43-1
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inquiry1. Well-equipped, stable and high-quality raw material supply chain, to provide customers with the best quality products. 2.Strict quality inspection process and professional certificate testing to ensure the quality level of the final product. 3.E
Cas:355-43-1
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inquirysuperior quality Appearance:liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package: 1kg/drum or 25kg/drum or as per your request. Application:Used as Pharmaceutical Intermediates Transportation:as per your request
Cas:355-43-1
Min.Order:1 Kilogram
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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
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inquiryCompany Introduction 1. Established in 2005, with two independent business divisions: Fine chemicals division; Pharmaceutical division. 2. Main product: Optical brightener Textile auxiliary Dye stuff Pigments
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A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
Cas:355-43-1
Min.Order:4 Kilogram
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inquiryProduct name: Perfluorohexyl Iodide CAS No.: 355-43-1 Molecule Formula:C6F13I Molecule Weight:445.95 Purity: 99.0% Package: 25kg/drum Description:White powder Manufacture Standards:Enterprise Standard TESTING ITEMS
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Min.Order:1 Kilogram
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Min.Order:1 Gram
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inquirypolytetrafluoroethylene
Pentafluoroethyl iodide
A
1-iodoheptadecafluorooctane
B
1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
C
n-perfluorohexyl iodide
D
1-Iodo-perfluorodecane
Conditions | Yield |
---|---|
at 100℃; for 5.13333h; Irradiation; Further byproducts given; | A 44.5% B 5% C 26.9% D 15.8% |
at 100℃; for 5h; Irradiation; | A 13.8% B 34.6% C 40.3% D 3.2% |
With copper at 90 - 100℃; for 5h; Product distribution; further reaction times, reagent ratio; | A 15.9% B 10.5% C 17.2% D 2.4% |
copper at 60 - 140℃; under 22502.3 - 33753.4 Torr; Product distribution / selectivity; |
polytetrafluoroethylene
Pentafluoroethyl iodide
A
1-iodoheptadecafluorooctane
B
1-iodoperfluorododecane
C
n-perfluorohexyl iodide
D
1-Iodo-perfluorodecane
Conditions | Yield |
---|---|
at 100℃; Further byproducts given; | A 44.5% B 5.8% C 26.9% D 5.8% |
at 100℃; for 5.13333h; Irradiation; Further byproducts given; | A 44.5% B 5.8% C 26.9% D 15.8% |
copper at 120℃; under 33753.4 Torr; Product distribution / selectivity; |
polytetrafluoroethylene
Pentafluoroethyl iodide
A
1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
B
n-perfluorohexyl iodide
Conditions | Yield |
---|---|
at 100℃; for 2h; Irradiation; | A 36.9% B 5.5% |
at 99.9℃; under 300.02 Torr; for 0.333333h; Rate constant; Quantum yield; Thermodynamic data; Irradiation; var. of partial pressures, temp., time, Ea; | A 36.6 % Chromat. B 11.3 % Chromat. |
polytetrafluoroethylene
1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
A
1-iodoheptadecafluorooctane
B
n-perfluorohexyl iodide
Conditions | Yield |
---|---|
mit UV Licht.Irradiation; |
polytetrafluoroethylene
1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
n-perfluorohexyl iodide
Conditions | Yield |
---|---|
im UV-Licht; | |
With bis(pentafluoropropionyl)peroxide at 28 - 70℃; for 0.333333h; Concentration; Temperature; Time; |
Conditions | Yield |
---|---|
With iodine In gas at 286.9 - 426.9℃; under 30 - 300 Torr; Equilibrium constant; |
polytetrafluoroethylene
1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
A
Pentafluoroethyl iodide
B
n-perfluorohexyl iodide
Conditions | Yield |
---|---|
at 29.9℃; under 300.02 Torr; for 6h; Rate constant; Quantum yield; Thermodynamic data; Irradiation; var. of partial pressures, time, Ea; | A 70.9 % Chromat. B 5.8 % Chromat. |
n-perfluorohexyl iodide
Conditions | Yield |
---|---|
With iodine |
polytetrafluoroethylene
iodotrifluoromethane
A
Pentafluoroethyl iodide
B
1,1,1,2,2,3,3-heptafluoro-3-iodo-propane
C
1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
D
undecafluoro-1-iodopentane
E
n-perfluorohexyl iodide
F
perfluoroheptyl iodide
Conditions | Yield |
---|---|
In gas Product distribution; Quantum yield; Thermodynamic data; Irradiation; pulsed CO2 laser; release of reaction enthalpy, selectivity depending on pressure and temperature; |
Conditions | Yield |
---|---|
With iodine In gas at 286.9 - 426.9℃; under 30 - 300 Torr; Equilibrium constant; |
Conditions | Yield |
---|---|
at 100 - 170℃; under 0.1 - 1 Torr; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
polytetrafluoroethylene
Pentafluoroethyl iodide
1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
A
1-iodoheptadecafluorooctane
B
n-perfluorohexyl iodide
Conditions | Yield |
---|---|
With diisopropyl peroxydicarbonate at 65 - 77℃; for 2h; Product distribution / selectivity; |
sodium 1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane-1-sulfinate
n-perfluorohexyl iodide
Conditions | Yield |
---|---|
With sodium persulfate; iodine In water; dimethyl sulfoxide at 20℃; for 1h; |
polytetrafluoroethylene
Pentafluoroethyl iodide
A
1-iodoheptadecafluorooctane
B
1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
C
n-perfluorohexyl iodide
Conditions | Yield |
---|---|
copper at 120℃; under 33753.4 Torr; Product distribution / selectivity; |
polytetrafluoroethylene
Pentafluoroethyl iodide
A
1-iodoheptadecafluorooctane
B
1-iodoperfluorododecane
C
1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
D
n-perfluorohexyl iodide
E
1-Iodo-perfluorodecane
Conditions | Yield |
---|---|
copper at 120℃; under 14251.4 - 33753.4 Torr; Product distribution / selectivity; |
polytetrafluoroethylene
1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
B
1-iodoheptadecafluorooctane
C
1-iodoperfluorododecane
D
n-perfluorohexyl iodide
E
1-Iodo-perfluorodecane
Conditions | Yield |
---|---|
copper at 110℃; under 2850.29 Torr; |
polytetrafluoroethylene
Bis(pentafluoraethyl)-fluorarsan
iodine
A
1-iodoheptadecafluorooctane
B
Pentafluoroethyl iodide
C
1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
D
n-perfluorohexyl iodide
Conditions | Yield |
---|---|
220°C, under pressure; | |
220°C, under pressure; |
polytetrafluoroethylene
Tris(pentafluoraethyl)arsan
iodine
A
1-iodoheptadecafluorooctane
B
Pentafluoroethyl iodide
C
1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
D
n-perfluorohexyl iodide
Conditions | Yield |
---|---|
220°C, under pressure; | |
220°C, under pressure; |
perfluorohexyliodine tetrafluoride
A
tetradecafluorohexane
B
n-perfluorohexyl iodide
polytetrafluoroethylene
1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
A
1-iodoheptadecafluorooctane
B
1-iodoperfluorododecane
C
n-perfluorohexyl iodide
D
1-Iodo-perfluorodecane
Conditions | Yield |
---|---|
copper Product distribution / selectivity; Reflux; |
1-iodoheptadecafluorooctane
Pentafluoroethyl iodide
A
1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
B
n-perfluorohexyl iodide
Conditions | Yield |
---|---|
at 490℃; for 0.00116667h; Product distribution / selectivity; |
A
n-perfluorohexyl iodide
B
1,1,3,3,4,4,5,5,6,6-decafluoro-6-iodo-1-hexene
C
1,1,3,3,4,4,5,5,6,6,8,8-dodecafluoro-1,7-octadiene
Conditions | Yield |
---|---|
With tributyl-amine at 48℃; for 1h; |
n-perfluorohexyl iodide
benzaldehyde
2,2,3,3,4,4,5,5,6,6,7,7,7-tridecafluoro-1-phenyl-1-hydroxyheptane
Conditions | Yield |
---|---|
Stage #1: n-perfluorohexyl iodide With methylmagnesium bromide In diethyl ether at -78℃; for 2h; Inert atmosphere; Stage #2: benzaldehyde In diethyl ether at -78℃; for 8h; Inert atmosphere; | 100% |
Stage #1: n-perfluorohexyl iodide With zirconocene dichloride; butyl magnesium bromide In 1,4-dioxane; diethyl ether at -78℃; for 1h; Inert atmosphere; Stage #2: benzaldehyde In 1,4-dioxane; diethyl ether at 20℃; for 1h; Reagent/catalyst; Inert atmosphere; chemoselective reaction; | 99% |
Stage #1: n-perfluorohexyl iodide With bis(cyclopentadienyl)titanium dichloride; isopropylmagnesium chloride In 1,4-dioxane; diethyl ether at -78 - -50℃; for 2h; Stage #2: benzaldehyde In 1,4-dioxane; diethyl ether at 20℃; for 1h; Reagent/catalyst; Temperature; | 99% |
n-perfluorohexyl iodide
allyl alcohol
2-iodo-4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluorononan-1-ol
Conditions | Yield |
---|---|
With mercury(I) iodide; mercury(II) iodide In N,N-dimethyl-formamide at 35℃; for 1.5h; | 100% |
zinc at 30℃; for 120h; Product distribution; also with various solvents; | 95% |
With zinc at 30℃; for 120h; | 95% |
Conditions | Yield |
---|---|
With 1-(2',2'-diphenylvinyl)pyrrolidine In dichloromethane at 20℃; for 16h; Reagent/catalyst; Irradiation; | 100% |
With pyrrolidine; Diphenylacetaldehyde In dichloromethane at 20℃; for 16h; Catalytic behavior; Reagent/catalyst; Wavelength; Inert atmosphere; Irradiation; | 99% |
With rose bengal; sodium thiosulfate In water; acetonitrile at 20℃; for 1h; Reagent/catalyst; Inert atmosphere; Irradiation; | 93% |
Vinylidene fluoride
n-perfluorohexyl iodide
1,1,1,2,2,3,3,4,4,5,5,6,6,8,8-pentadecafluoro-8-iodooctane
Conditions | Yield |
---|---|
Heating; | 100% |
at 180℃; |
n-perfluorohexyl iodide
perfluorohexyliodine tetrafluoride
Conditions | Yield |
---|---|
With xenon difluoride; boron trifluoride In various solvent(s) at -5 - 25℃; | 100% |
(pentamethylcyclopentadienyl)(dicarbonyl)iridium(I)
n-perfluorohexyl iodide
Cp(*)Ir(CO)(n-C6F13)I
Conditions | Yield |
---|---|
In dichloromethane I(CF2)5CF3 added dropwise to a soln. of Ir complex, stirred for 15 min under N2; solvent-removed, washed (hexane); elem. anal.; | 100% |
diethoxyphosphoryl-acetic acid ethyl ester
n-perfluorohexyl iodide
ethyl 4-(trifluoromethyl)benzoate
Conditions | Yield |
---|---|
Stage #1: n-perfluorohexyl iodide; ethyl 4-(trifluoromethyl)benzoate With methyllithium; lithium bromide In diethyl ether at -80℃; for 0.5h; Horner-Wadsworth-Emmons Olefination; Inert atmosphere; Stage #2: With diethylaluminium chloride In diethyl ether at -80℃; for 0.25h; Horner-Wadsworth-Emmons Olefination; Inert atmosphere; Stage #3: diethoxyphosphoryl-acetic acid ethyl ester With triethylamine; lithium bromide In tetrahydrofuran; diethyl ether at 20℃; for 3h; Horner-Wadsworth-Emmons Olefination; Inert atmosphere; stereospecific reaction; | 100% |
n-perfluorohexyl iodide
1,2-dibromo-4,5-dimethylbenzene
Conditions | Yield |
---|---|
With copper In dimethyl sulfoxide at 110℃; for 22h; Inert atmosphere; Schlenk technique; | 100% |
With copper In dimethyl sulfoxide at 110℃; for 22h; Inert atmosphere; | 97% |
n-perfluorohexyl iodide
1-allyl-3-methoxybenzene
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0) In hexane at -78 - 20℃; for 36h; Inert atmosphere; | 100% |
allylsuccinic anhydride
n-perfluorohexyl iodide
3-(perfluorohexyl)-2-iodopropyl-2-butane-1,4-dioic acid anhydride
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) at 70 - 92℃; for 7h; | 99.6% |
n-perfluorohexyl iodide
4-(perfluorohexyl)-3-iodo-2-butyl-2-butane-1,4-dioic acid anhydride
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) at 72 - 84℃; for 6h; | 99.4% |
n-perfluorohexyl iodide
3,4-epoxy-1-tetradecene
(E)-1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-icos-8-en-10-ol
Conditions | Yield |
---|---|
With triethyl borane In hexane; benzene at 25℃; for 17h; Product distribution; The reaction of 1,3-diene monoxide with different radical sources in the presence of Et3B provides 4-substituted-2-buten-1-ol in good yield with a novel synthetic route.; | 99% |
With triethyl borane In hexane; benzene at 25℃; for 17h; | 99% |
Conditions | Yield |
---|---|
With pyrrolidine; Diphenylacetaldehyde In dichloromethane at 20℃; for 16h; Inert atmosphere; Irradiation; | 99% |
With sodium triethylborohydride In hexane for 6h; Ambient temperature; | 82.8% |
n-perfluorohexyl iodide
(3aR,5R,6S,6aR)-6-(allyloxy)-5-((R)-2,2-dimethyl[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxole
Conditions | Yield |
---|---|
With sodium dithionite; sodium hydrogencarbonate In water; acetonitrile for 0.5h; Ambient temperature; | 99% |
n-perfluorohexyl iodide
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; copper In fluorobenzene; dimethyl sulfoxide at 80℃; for 72h; | 99% |
Conditions | Yield |
---|---|
Stage #1: 1-hexene; n-perfluorohexyl iodide In acetic acid Heating; Stage #2: 2-methoxy-1,4-naphthoquinone With dibenzoyl peroxide In acetic acid Heating; | 99% |
Conditions | Yield |
---|---|
With dibenzoyl peroxide In acetic acid for 4h; Heating; | 99% |
tris(allyl)borate
n-perfluorohexyl iodide
A
2-iodo-4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluorononan-1-ol
B
allyl alcohol
Conditions | Yield |
---|---|
Stage #1: tris(allyl)borate; n-perfluorohexyl iodide With 2,2'-azobis(isobutyronitrile) at 60 - 70℃; for 3h; Stage #2: With water at 60℃; | A 99% B n/a |
n-perfluorohexyl iodide
tris-iso-propylsilyl acetylene
(Z)-3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-1-iodo-1-triisopropylsilyl-1-octene
Conditions | Yield |
---|---|
With zinc In dichloromethane for 2h; Reflux; stereoselective reaction; | 99% |
n-perfluorohexyl iodide
methyl methacrylate
Ethyl 2-methyl-4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluorononanoate
Conditions | Yield |
---|---|
With tris-(trimethylsilyl)silane; sodium thiosulfate In dichloromethane; water at 20℃; for 4h; UV-irradiation; Sealed tube; | 99% |
Conditions | Yield |
---|---|
With 2,4,6-trimethyl-pyridine; (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis-(2-phenylpyridine(-1H))-iridium(III) hexafluorophosphate; ascorbic acid In dimethyl sulfoxide at 23 - 25℃; for 2h; Inert atmosphere; Irradiation; | 99% |
n-perfluorohexyl iodide
p-aminoiodobenzene
4-(1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexyl)phenylamine
Conditions | Yield |
---|---|
With copper In dimethyl sulfoxide at 120℃; for 10h; | 98.5% |
With copper In dimethyl sulfoxide at 120℃; for 2h; | 86% |
With copper In dimethyl sulfoxide at 120℃; | 84.27% |
1-dodecene
n-perfluorohexyl iodide
1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluoro-8-iodooctadecane
Conditions | Yield |
---|---|
With diethylamine; 1,1'-bis-(diphenylphosphino)ferrocene; bis(benzonitrile)palladium(II) dichloride In water at 20℃; for 1h; Kharasch reaction; | 98% |
With triethyl borane In hexane at 25℃; for 3.5h; | 93% |
With sodium acetate In neat (no solvent) at 140℃; for 24h; Kharash-Sosnovsky Allylic Oxidation; Green chemistry; | 85% |
n-perfluorohexyl iodide
perfluoroethanesulfonic acid
1,1,2,2,2-Pentafluoro-ethanesulfonic acid tridecafluorohexyl ester
Conditions | Yield |
---|---|
at 25℃; anodic oxidation; | 98% |
byproducts: I2; Electrochem. Process; in the acid; | 98% |
byproducts: I2; Electrochem. Process; in the acid; | 98% |
Conditions | Yield |
---|---|
In water for 2h; Ambient temperature; electrocatalysis; carbon fibre cathode, carbon rod anode, sat. KCl electrolyt; | 98% |
n-perfluorohexyl iodide
Conditions | Yield |
---|---|
With sodium dithionite; sodium hydrogencarbonate In water; acetonitrile for 0.5h; Ambient temperature; | 98% |
n-perfluorohexyl iodide
(2R,4aR,6S,7R,8S,8aR)-7,8-Bis-allyloxy-2-phenyl-6-phenylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxine
Conditions | Yield |
---|---|
With sodium dithionite; sodium hydrogencarbonate In water; acetonitrile for 0.5h; Ambient temperature; | 98% |
3,4-di-O-allyl-1,2:5,6-di-O-isopropylidene-D-mannitol
n-perfluorohexyl iodide
1,2:5,6-di-O-isopropylidene-3,4-di-O-(4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-2-iodononyl)-D-mannitol
Conditions | Yield |
---|---|
With air; triethyl borane In hexane at 0 - 20℃; for 1.16667h; Addition; | 98% |
Conditions | Yield |
---|---|
With dibenzoyl peroxide In acetic acid for 4h; Heating; | 98% |
n-perfluorohexyl iodide
1-(3-butenyl)-4-bromobenzene
1-bromo-4-(5,5,6,6,7,7,8,8,9,9,10,10,10-tridecafluoro-3-iododecyl)benzene
Conditions | Yield |
---|---|
With sodium metabisulfite; 2,2'-azobis(isobutyronitrile) at 80℃; for 4h; | 98% |
With sodium metabisulfite; 2,2'-azobis(isobutyronitrile) at 80℃; for 4h; | 98% |
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