Dayangchem’s 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. DayangChem can provide different quantiti
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inquiry1,1,2,2-Tetrachloroethane Basic information Product Name: 1,1,2,2-Tetrachloroethane Synonyms: (CHCl2)2;1,1,2,2,-tetrachlor-ethane;1,1,2,2-Czterochloroetan;1,1,2,2-czterochloroetan(polish
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inquiryISO Appearance:Colorless liquid Storage:In cool and dry place Package:300kg per plastic drum,80drum per container Application:Used in the production of metal net lotion, pesticides, herbicides, solvents, etc Transportation:According to customers're
Henan 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
Hangzhou 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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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
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
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inquiryProduct Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
Superior quality, moderate price & quick delivery. Appearance:colorless transparent liquid Storage:stored in a cool, dry and ventilated place to provent sun and rain Package:25kg/drum, or as per your request. Application:Used in organic syn
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Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
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Top sale 79-34-5 1,1,2,2-Tetrachloroethane Application:Top sale 79-34-5 1,1,2,2-Tetrachloroethane
Top sale 79-34-5 1,1,2,2-TetrachloroethaneAppearance:liquid Storage:keep dry Package:25kg/bag or follow your requirement Application:pharmaceutical intermediates Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. By ai
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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
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Min.Order:10 Milligram
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inquiry
Cas:79-34-5
Min.Order:1 Kilogram
Negotiable
Type:Trading Company
inquiryProduct name : 1,1,2-Trichloroethane Chemical Name : 1.1.2.2-Tetrachloroethane Molecular Formula : CHCL2CHCL2 Molecular Weight : 167.85 Appearance :
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Min.Order:200 Kilogram
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inquiryFOB Price: US $ 1 - 5 / Kilogram Appearance:colorless transparent liquid Storage:Store in a cool, dry and well-ventilated warehouse Package:Package: 200 L plastic drum ,net weight 300 kg/drum Application:Used as solvent, metal lotion ,etc. for med
Profile Hebei Ruishun Trade Co.LTD, registered capital of $1 million ,have a production of pharmaceutical raw materials, pharmaceutical raw materials factory reagent r&d center,Seek development by credit reputation. Our products have a large
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inquiryAt Share Chemical Company, we scrupulously abide by our policy of “Excellent Quality at a Reasonable Price”. We strive to satisfy all of our customers by providing the finest quality products supported by the finest in customer servi
Conditions | Yield |
---|---|
With 2,3-dimethylbutane In benzene at 20℃; Irradiation; | 94% |
With chlorine at 80 - 95℃; unter Ausschluss von Sauerstoff; |
C11H16Cl10NO3P
A
bis(2,2,2-trichloroethyl) piperidinophosphonate
B
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
at 180℃; under 0.03 Torr; | A 89% B 93% |
C10H14Cl10NO4P
A
bis(2,2,2-trichloroethyl) morpholinophosphonate
B
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
at 180℃; under 0.03 Torr; | A 87% B 93% |
N,N-Dichlorobenzenesulfonamide
1,2-Dichloroethylene
A
benzenesulfonamide
B
N-(2,2-dichloroethylidene)benzenesulfonamide
C
N-{2,2-dichloro-1-[(phenylsulfonyl)amino]ethyl}benzenesulfonamide
D
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
at 47 - 55℃; for 10h; Irradiation; Further byproducts given. Yields of byproduct given; | A n/a B n/a C 80.7% D n/a |
(2-Chlor-vinyl)-dimethyl-chlorsilan
A
1,2-Dichloroethylene
B
dimethylsilicon dichloride
C
Chloro-dimethyl-(1,2,2-trichloro-ethyl)-silane
D
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
With chlorine for 5h; Further byproducts given; | A 5% B 6% C 70% D 2% |
N,N-Dichlorobenzenesulfonamide
1,2-Dichloroethylene
A
1,1,2,2-tetrachloroethylene
B
Trichloroethylene
C
N-(2,2,2-trichloroethylidene)benzenesulfonamide
D
N-(2,2-dichloroethylidene)benzenesulfonamide
E
N-{2,2-dichloro-1-[(phenylsulfonyl)amino]ethyl}benzenesulfonamide
F
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
at 55℃; for 22h; Product distribution; other time, other temperature, other initiator; | A n/a B n/a C n/a D n/a E 54.1% F n/a |
1,2-Dichloroethylene
N,N-dichloro-4-chlorobenzenesulfonamide
A
N-(2,2-dichloroethylidene)-p-chlorobenzenesulfonamide
B
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
for 4h; Irradiation; | A 50% B n/a |
N,N-Dichlorobenzenesulfonamide
1,2-Dichloroethylene
A
N-(2,2-dichloroethylidene)benzenesulfonamide
B
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
for 4h; Irradiation; | A 45% B n/a |
β-chlorovinyltrimethylsilane
A
chloro-trimethyl-silane
B
1,2-Dichloroethylene
D
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
With chlorine for 5h; Further byproducts given; | A 10% B 7% C 45% D 3% |
β-chlorovinyltrimethylsilane
A
1,2-Dichloroethylene
B
Trimethyl-(pentachlorethyl)-silan
D
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
With chlorine for 5h; Further byproducts given; | A 7% B 14% C 45% D 3% |
N,N-dichloro-p-toluenesulfonamide
1,2-Dichloroethylene
A
N-(2,2,2-trichloroethyliden)-p-toluenesulfonamide
B
Trichloroethylene
C
N-(2,2-dichloro-1-{[(4-methylphenyl)sulfonyl]amino}ethyl)-4-methylbenzenesulfonamide
D
toluene-4-sulfonamide
E
N-[2,2-Dichloro-eth-(E)-ylidene]-4-methyl-benzenesulfonamide
F
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
at 55℃; for 22h; Product distribution; other time, other temperature, other initiator; | A n/a B n/a C 44.1% D n/a E n/a F n/a |
Conditions | Yield |
---|---|
With hexacarbonyl molybdenum at 140℃; for 3h; further reagent Fe(CO)5; | A 42% B 23% |
With iron pentacarbonyl at 140℃; for 3h; further reagent Mo(CO)6; | A 27% B 23% |
1,2-Dichloroethylene
N,N-dichloro-4-chlorobenzenesulfonamide
A
1,1,2,2-tetrachloroethylene
B
4-Chlorobenzenesulfonamide
C
N-(2,2,2-trichloroethylidene)-4-chlorobenzenesulfonamide
D
N-(2,2-dichloroethylidene)-p-chlorobenzenesulfonamide
E
N-<2,2-dichloro-1-(N-p-chlorobenzenesulfonamido)ethyl>-p-chlorobenzenesulfonamide
F
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
at 55℃; for 22h; Product distribution; other time, other temperature, other initiator; | A n/a B n/a C n/a D n/a E 40.4% F n/a |
4-Phenylbutyric acid
A
Propylbenzene
B
1,6-diphenylhexane
D
1-fluoro-3-phenylpropane
E
1-fluoro-1-phenylpropane
F
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
With xenon fluoride In dichloromethane at 20℃; for 14 - 18h; Inert atmosphere; | A 18% B 11% C 12% D 32% E 6% F 14% |
chloroform
aniline
A
dichloromethane
B
phenyl isocyanate
C
Azobenzene
D
N-phenylphenylene-1,4-diamine
E
N-phenyl-1,2-benzenediamine
F
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
at 15℃; for 24h; Product distribution; Mechanism; Irradiation; | A n/a B 30.2% C 12.5% D 10.5% E 18.4% F n/a |
Conditions | Yield |
---|---|
With chlorine at 80 - 95℃; unter Ausschluss von Sauerstoff; | |
With sulfuryl dichloride; dibenzoyl peroxide |
diethyl ether
hexachloroethane
ethylmagnesium bromide
A
1,1,2,2-tetrachloroethylene
B
1,1,1,2-tetrachoroethane
C
pentachloroethane
D
1,1,2,2-tetrachloroethane
diethyl ether
hexachloroethane
A
1,1,2,2-tetrachloroethylene
B
1,1,1,2-tetrachoroethane
C
pentachloroethane
D
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
With chlorine im UV-Licht; |
Conditions | Yield |
---|---|
With hydrogenchloride; kieselguhr; air; copper dichloride |
chloroform
A
tetrachloromethane
B
1,1,2,2-tetrachloroethylene
C
pentachloroethane
D
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
beim Durchgang des elektrischen Lichtbogens; weitere Produkten: Hexachloraethan, Hexachlorbenzol, HCl und Kohle; |
1,1,2-trichloro-2-iodo-ethane
A
1,2-Dichloroethylene
B
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
bei der Destillation; |
Trichloroethylene
A
1,1,2,2-tetrachloroethylene
B
1,1,2,4,4-pentachloro-1,3-butadiene
C
1,1,1,2-tetrachoroethane
D
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
at 200 - 250℃; under 934095 Torr; Produkt5:Pentachloraethan.Pyrolysis; |
Conditions | Yield |
---|---|
With phosphorus pentachloride |
1-chloro-2-dichloroiodanyl-ethene
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
With aluminium trichloride at 70 - 75℃; Einleiten Chlor und gleichzeitig Acetylen,auschliessend jede Spur von Luft; |
diethyl ether
hexachloroethane
para-methylphenylmagnesium bromide
A
1,1,2,2-tetrachloroethylene
B
1,1,1,2-tetrachoroethane
C
pentachloroethane
D
1,1,2,2-tetrachloroethane
diethyl ether
hexachloroethane
1-naphthylmagnesiumbromide
A
1,1,2,2-tetrachloroethylene
B
1,1,1,2-tetrachoroethane
C
pentachloroethane
D
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
With chlorine | |
With chlorine; 1,1,2,2-tetrachloroethane | |
With chlorine; iron(III) chloride |
Conditions | Yield |
---|---|
With chlorine; iron(III) chloride; 1,1,2,2-tetrachloroethane at 135℃; |
Conditions | Yield |
---|---|
In water; butan-1-ol mixing Cu(OH)2 and amine in n-BuOH, stirring (room temp., 10 min), addn.of C2H2Cl4, refluxing (8 h; pptn.), addn. of water, stirring, sepd. of aq. layer, filtration of aq. layer, washing (n-BuOH), crystn. on volume reduction and standing (refrigerator); treating of crude product with mixt. of ether/benzene (1/1) on filtration paper, washing (ether), drying (reduced pressure); elem. anal.; | 95.6% |
Conditions | Yield |
---|---|
In water; butan-1-ol refluxing in butanol (10 h), extraction (water); pptn. from aq. phase (concn., cooling); elem. anal.; | 95% |
Conditions | Yield |
---|---|
With hydrogen fluoride; antimonypentachloride at 80 - 90℃; Autoclave; | 92.3% |
With hydrogen fluoride; antimonypentachloride; chlorine at 120℃; |
Conditions | Yield |
---|---|
at 140℃; for 72h; | 92% |
Conditions | Yield |
---|---|
at 140℃; for 72h; | 91% |
1-naphthol-2-sulfonic acid
1,1,2,2-tetrachloroethane
4-hydroxy-naphthalene-1,3-disulfonic acid
Conditions | Yield |
---|---|
90% |
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
With N-Bromosuccinimide; dibenzoyl peroxide | 90% |
trans-[Cl2(pyrazine)4ruthenium(II)]
silver trifluoromethanesulfonate
butan-1-ol
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
In 1,1,2,2-tetrachloroethylene; butan-1-ol a soln. of Ag salt (n-butanol) added dropwise to a soln. of Ru compd. (TCE), stored for 1 h; ppt. filtered, washed (n-butanol), dried (vac., 3 h); elem. anal.; | 90% |
iron(II) acetate
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
With acetic anhydride In acetic acid stirring at 100°C for ca. 1 h in 1:1 mixture of AcOH and CHCl2CHCl2; evapn., dissolution in CHCl2CHCl2, filtration, evapn.; elem. anal.; | 90% |
1,1,2,2-tetrachloroethane
1,2,2-trichloroethyl fluosulfate
Conditions | Yield |
---|---|
With chlorine fluorosulfate 1.) -30 deg C, 1 h, 2.) 20 deg C, 2.5 h, 3.) 60 deg C, 1 h; | 88.7% |
Conditions | Yield |
---|---|
In butan-1-ol byproducts: HCl; equimolar mixt. of Ni(OH)2, 1,1,2,2-tetrachloroethane and 1,3-diaminopropane in n-butanol stirred at room temp.; refluxed for ca. 8 h; stirred for ca. 12 min with water; filtered; aq. layer of filtrate sepd.; concd.; refrigerated; crystals washed with n-butanol and petroleum ether; elem. anal.; | 88% |
dichlorotetrakis(triphenylphosphine)ruthenium(II)
2,3-S(C2H4S)2-1,4-Me2C10H4
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
In diethyl ether under Ar atm. mixt. ligand and (RuCl2(PPh3)4) in Et2O at room temp. for 5 min; ppt. was extd. with CH2Cl2, solvent was evapd, residue was crystd. from 1,1,2,2-tetrachloroethane-Et2O; elem. anal.; | 88% |
Conditions | Yield |
---|---|
In butan-1-ol byproducts: HCl; Ni(OH)2 added to soln. of 1,1,2,2-tetrachloroethane and 1,2-diaminoethane (molar ratio 1:1:1) in n-butanol; stirred and refluxed for ca. 7 h; cooled; stirred for ca. 10 min with water; filtered; aq. layer of filtrate sepd.; concd.; refrigerated; crystals washed with n-butanol and petroleum ether; elem. anal.; | 86% |
1,2-dimethoxybenzene
4-chloro-benzoyl chloride
1,1,2,2-tetrachloroethane
4-chloro-3',4'-dimethoxy benzophenone
Conditions | Yield |
---|---|
With FeCl3; graphite | 84.3% |
With FeCl3; graphite | 84.3% |
graphite | 81.3% |
N-allyl-N-phenyl-2-methacrylamide
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
With tris(2,2'-bipyridyl)ruthenium dichloride; 4-methoxybenzenediazonium tetrafluoroborate; sodium carbonate In neat (no solvent) at 50℃; for 20h; Inert atmosphere; Schlenk technique; Irradiation; | A 83% B n/a |
1,2-dimethoxybenzene
4-chlorotrichloromethylbenzene
1,1,2,2-tetrachloroethane
4-chloro-3',4'-dimethoxy benzophenone
Conditions | Yield |
---|---|
graphite In water | 79.5% |
Conditions | Yield |
---|---|
With tetrakis(acetonitrile)copper(I)tetrafluoroborate; 4-methoxybenzenediazonium tetrafluoroborate; sodium carbonate at 80℃; for 6h; Schlenk technique; Inert atmosphere; | 77% |
Conditions | Yield |
---|---|
With hydrogenchloride; oxygen at 379.84℃; Reagent/catalyst; Temperature; | 74.3% |
With chlorine at 379.84℃; Gas phase; chemoselective reaction; | 57.3% |
at 350 - 400℃; bei der Einwirkung von Luft; |
bis(N,N'-diphenyl-2,4-pentanediiminato)chromium(II)
1,1,2,2-tetrachloroethane
bis(N,N'-diphenyl-2,4-pentanediiminato)chlorochromium(III)
Conditions | Yield |
---|---|
In diethyl ether standard Schlenk techniques; tetrachloroethane added to soln. of Cr complex (molar ratio 1:2) in Et2O with stirring; stirred overnight; solvent evapd.; extd. with Et2O; evapd. slowly at room temp.; elem. anal.; | 73% |
Conditions | Yield |
---|---|
In carbon dioxide; N,N-dimethyl-formamide | 70% |
1,1,2,2-tetrachloroethane
A
1,1,2,2-tetrachloroethylene
B
Trichloroethylene
Conditions | Yield |
---|---|
With hydrogenchloride; oxygen at 379.84℃; for 18h; | A 20.8% B 64.3% |
With CuCl2/KCl/attapulgite; chlorine at 379.84℃; Gas phase; chemoselective reaction; | A 16.6% B 45% |
1,1,2,2-tetrachloroethane
A
1,1,2,2-tetrachloroethylene
B
Trichloroethylene
C
pentachloroethane
Conditions | Yield |
---|---|
With hydrogenchloride; oxygen at 379.84℃; | A 20.8% B 64.3% C 6.1% |
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
In 1,3,5-trimethyl-benzene at 170℃; for 18h; Inert atmosphere; Schlenk technique; | 60% |
Conditions | Yield |
---|---|
Stage #1: oxalic acid; 1,1,2,2-tetrachloroethane With sulfuric acid for 10h; Stage #2: With sulfur trioxide; mercury(II) sulfate at 60℃; | 58.8% |
Conditions | Yield |
---|---|
56% |
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