Dayang Chem (Hangzhou) Co.,Ltd.
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:7783-61-1
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryAlity 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
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
Cas:7783-61-1
Min.Order:5 Kiloliter
FOB Price: $1.2 / 5.0
Type:Manufacturers
inquiryHangzhou J&H Chemical Co., Ltd.
J&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
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
Cas:7783-61-1
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquiryHunan chemfish Pharmaceutical co.,Ltd
7783-61-1 Appearance:95%+ Package:R&D,Pilot run Application:7783-61-1 Transportation:per client require Port:Express ,Air, Sea
Kono Chem Co.,Ltd
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
Henan Allgreen Chemical Co.,Ltd
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
Zhuozhou Wenxi import and Export Co., Ltd
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:7783-61-1
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiryAntimex 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
Henan Tianfu Chemical Co., Ltd.
Best price,High quality Storage:Room Temperature Application:For Pharmacy Chemicals Transportation:by sea,air
Hunan Russell Chemicals Technology Co.,Ltd
high 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
Amadis Chemical Co., Ltd.
1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G
Cas:7783-61-1
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiryHuBei Ipure Biotech CO.,ltd
HuBei ipure is a diversified product production and operation enterprise, with API, pharma intermediates, and other fine chemicals as well as R&D and pigments development and sales as one of the large enterprises, with more than 130 acres of pl
Cas:7783-61-1
Min.Order:1 Gram
FOB Price: $1.0 / 2.0
Type:Trading Company
inquiryShanghai 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
Nanjing Raymon Biotech Co., Ltd.
Silane, tetrafluoro- Storage:keep in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/pharma intermediate Transportation:By Sea,by Air,By courier like DHL or Fedx. Port:Shanghai/Shenzhen
Synova( Tianjin ) Chemical Technology Co,.Ltd
The company have effective management team, professional technical R & D personnel, the service spirit of customer oriented. We have long-term cooperation with famous domestic manufacturer, and excellent customer resources overseas. We are skilled in
Skyrun Industrial Co.,Ltd
Good Price, prompt shipment Application:Catalytic agent; Petrochemical additive; Used in organic synthesis
Hebei Ruishun Trade Co.,Ltd
Supply top quality products with a reasonable price Application:api
Asia Pacific Gas Enterprise Company Limited
Purity Grade customized Formula SiF4 Application This volatile compound finds limited use in microelectronics and organic synthesis. Mol…
NovaChemistry
high purity Application:Drug intermediates Materials intermediates and active molecules
Synthetic route
-
-
116-14-3
polytetrafluoroethylene
-
-
4168-07-4
(1,1,2,2-tetrafluoroethyl)trifluorosilane
-
A
-
433-66-9
pentafloropropylene
-
B
-
931-91-9
1,1,2,2,3,3-Hexafluoro-cyclopropane
-
C
-
379-14-6
1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane
-
D
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| at 150℃; for 18h; Further byproducts given; | A 5% B n/a C 74% D 100% |
| at 200℃; for 10h; Further byproducts given; | A 19% B n/a C 71% D 98% |
-
-
4168-07-4
(1,1,2,2-tetrafluoroethyl)trifluorosilane
-
A
-
433-66-9
pentafloropropylene
-
B
-
379-14-6
1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane
-
C
-
7783-61-1
silicon tetrafluoride
-
D
-
359-11-5
1,1,2-trifluoroethylene
| Conditions | Yield |
|---|---|
| With polytetrafluoroethylene at 150℃; for 18h; Further byproducts given; | A 5% B 74% C 100% D 10% |
-
-
353-50-4
Carbonyl fluoride
-
-
112926-00-8, 7631-86-9
silica gel
-
A
-
124-38-9
carbon dioxide
-
B
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| In neat (no solvent) slight excess over the stoich. amt. of COF2 required; reaction mixt. heated in a stainless steel or monel cylinder at 160°C for 36 h; | A n/a B 100% |
-
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| In neat (no solvent) salt dried at 250°C in vac. or in N2 flow; thermal dissocn. at 500-620°C in vac. in stainless steel reactor; fed into metallic cylinder cooled with liq. N2; filtration, IR, atomic emission and mass spectrometry; | 100% |
| With water In neat (no solvent) byproducts: Si2OF6, SiF3OH, SiF3H; predrying of Na2SiF6 at 250-300.C in vac. or N2 for several hours, heating at 500 to 620°C in stainless steel reactor; cooling with liquid N2; | |
| With sulfuric acid In sulfuric acid reaction by use of concd. H2SO4;; |
-
-
54939-02-5
(2,2-dichloro trifluoro ethyl) trifluoro silane
-
A
-
79-35-6
1,1'-dichloro-2,2'-difluoroethene
-
B
-
598-88-9
1,2-dichloro-1,2-difluoroethene
-
C
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| In neat (no solvent) pyrolysis at 140°C, 3 hours;; | A 8% B 90% C 100% |
| In neat (no solvent) pyrolysis at 140°C, 3 hours;; | A 8% B 90% C 100% |
-
-
6651-55-4
diphenylfluorostibine
-
-
368-47-8
phenyltrifluorosilane
-
A
-
603-36-1
triphenylantimony
-
B
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| reflux for 3 d; | A 100% B n/a |
| reflux for 3 d; | A 100% B n/a |
-
-
563-79-1
2,3-Dimethyl-2-butene
-
-
4168-07-4
(1,1,2,2-tetrafluoroethyl)trifluorosilane
-
A
-
17216-38-5
1-fluoro-1-difluoromethyl-2,2,3,3-tetramethylcyclopropane
-
B
-
7783-61-1
silicon tetrafluoride
-
C
-
359-11-5
1,1,2-trifluoroethylene
| Conditions | Yield |
|---|---|
| at 150℃; for 16h; | A 86% B 99% C 6% |
-
-
379-14-6
1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane
-
-
110-83-8
cyclohexene
-
A
-
116-14-3
polytetrafluoroethylene
-
B
-
433-66-9
pentafloropropylene
-
C
-
201230-82-2
carbon monoxide
-
D
-
115-25-3
Octafluorocyclobutane
-
E
-
823-70-1
7,7-difluoronorcarane
-
F
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| With Pyrex tube at 200℃; for 320h; Product distribution; Mechanism; further periods of contact time, other temperatures; | A 14% B 99% C 11% D n/a E 47% F 13% |
-
-
116-14-3
polytetrafluoroethylene
-
-
4168-07-4
(1,1,2,2-tetrafluoroethyl)trifluorosilane
-
A
-
433-66-9
pentafloropropylene
-
B
-
379-14-6
1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane
-
C
-
7783-61-1
silicon tetrafluoride
-
D
-
359-11-5
1,1,2-trifluoroethylene
| Conditions | Yield |
|---|---|
| at 200℃; for 10h; Further byproducts given; | A 19% B 71% C 98% D 8% |
-
-
75-44-5
phosgene
-
A
-
353-50-4
Carbonyl fluoride
-
B
-
353-49-1
fluoroformyl chloride
-
C
-
124-38-9
carbon dioxide
-
D
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| In acetonitrile condensation, 20°C in a sealed Pyrex tube, staying 24 h at 20°C; | A 97% B 0% C n/a D <1 |
-
-
18114-91-5
Caesium-trans-bis(trifluormethyl)-tetrafluorphosphat
-
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| With glass; acid In not given | 97% |
-
-
513-35-9
2-methyl-but-2-ene
-
-
4168-07-4
(1,1,2,2-tetrafluoroethyl)trifluorosilane
-
A
-
7783-61-1
silicon tetrafluoride
-
B
-
359-11-5
1,1,2-trifluoroethylene
-
-
17287-40-0, 17287-41-1, 74755-46-7, 74755-47-8
1-fluoro-r-1-difluoromethyl-c-2,3-t-2-trimethylcyclopropane
-
-
17287-40-0, 17287-41-1, 74755-46-7, 74755-47-8
1-fluoro-r-1-difluoromethyl-c-2-t-2,3-trimethylcyclopropane
| Conditions | Yield |
|---|---|
| at 150℃; for 18h; Further byproducts given; | A 96% B 16% C 34% D 47% |
-
-
6651-55-4
diphenylfluorostibine
-
-
1840-40-0
trichloromethyltrifluorosilane
-
A
-
21907-22-2
diphenylantimony trichloride
-
B
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| at 15°C; | A n/a B 90% |
| at 15°C; | A n/a B 90% |
-
-
681-84-5
tetramethylorthosilicate
-
-
124-28-7
N,N-dimethyl-n-octadecylamine
-
-
375-72-4
Nonafluorobutanesulfonyl fluoride
-
A
-
7783-61-1
silicon tetrafluoride
-
B
-
25628-14-2
N,N,N,-trimethyloctadecyl ammonium nonafluorobutanesulfonate
| Conditions | Yield |
|---|---|
| In tetrahydrofuran 50°C , 6 h; | A n/a B 84% |
| In tetrahydrofuran 50°C , 6 h; | A n/a B 84% |
-
-
7783-56-4
antimony(III) fluoride
-
-
4109-96-0
Dichlorosilane
-
A
-
13824-36-7
difluorosilane
-
B
-
13465-71-9
trifluorosilane
-
C
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| In neat (no solvent) byproducts: H2; reaction in presence of SbCl5 at room temperature;; | A 80% B n/a C 10% |
-
-
7783-56-4
antimony(III) fluoride
-
-
4109-96-0
Dichlorosilane
-
A
-
13824-36-7
difluorosilane
-
B
-
1333-74-0
hydrogen
-
C
-
13465-71-9
trifluorosilane
-
D
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| In neat (no solvent) fluorination of SiH2Cl2 with SbF3 at room temp. for a longer period of time;; | A 80% B n/a C n/a D n/a |
-
-
13830-68-7
disilicon hexafluoride
-
-
1631-73-8
trimethylstannane
-
A
-
15195-26-3
F3SiSiH3
-
B
-
126087-12-5
trimethyl(trifluorsilyl)stannane
-
C
-
13465-71-9
trifluorosilane
-
D
-
7783-61-1
silicon tetrafluoride
-
E
-
18365-37-2
Trimethylstannylsilan
| Conditions | Yield |
|---|---|
| In neat (no solvent) N2 atmosphere, high vac. line; condensing, warming (room temp., 1.5 h); passing through traps (-78°C and -46°C); | A n/a B 77% C n/a D n/a E 5% |
| Conditions | Yield |
|---|---|
| In melt placing of mixt. of Si with SnF2 (molar ratio SnF2:Si=2.00) in Fluoroplast-4 ampule, closing by screwed stopper, exposition for 1.00 h at 250°C; various product ratio yields for various conditions; cooling, stirring up in water, collection, drying; | A 76.8% B n/a |
-
-
41066-09-5
hexafluorodisilthiane
-
C
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| In neat (no solvent) byproducts: CF3SiBr; under dry N2, in a sealed tube, 60 h at room temp., molar ratio of silane and HBr was 1:1, an other non-volatile product was also formed; fractionated distn. at a low-temp. column, S-compds. were trapped at 143K, SiF4 at 77 K; | A n/a B 68% C 1% |
-
-
359-55-7
iodo-bis-trifluoromethyl-arsine
-
A
-
359-54-6
bis(trifluoromethyl)fluoroarsine
-
B
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| with well dried AgF; | A 60% B n/a |
| with well dried AgF; | A 60% B n/a |
-
-
13517-13-0
disilicon hexabromide
-
A
-
13830-68-7
disilicon hexafluoride
-
B
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| In 1,2-dichloro-ethane; acetonitrile Si2Cl6 dissolved in C2H4Cl2 added dropwise over 2 h to suspn. of KF in boiling MeCN, allowed to reflux for 30 min in slow stream of N2; gaseous products trapped in cooled (liq. N2) trap, anlyzed by IR; | A 60% B n/a |
-
-
16865-60-4
iodo-trifluoro-silane
-
A
-
41066-09-5
hexafluorodisilthiane
-
C
-
14515-39-0
hexafluorodisiloxane
-
D
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| In neat (no solvent) byproducts: HgI2; CF3SiI:HgS molar ratio was 1:2, in a sealed tube, 300 K for 7 days, under dry N2; low temp. fractionated distn., less volatile fraction was purified by passing it through a 198 K trap into a trap held at 173 K, the (F3SiS)2SiF2 was identified by NMR, its purity was 98 %;; | A 54% B n/a C 1% D n/a |
-
-
22687-88-3
(1,2-dibromotrifluoroethyl)pentafluorosulfur(VI)
-
A
-
640723-20-2, 2699-79-8, 12769-73-2
fluorosulfonyl fluoride
-
B
-
5714-22-7
disulfur decafluoride
-
C
-
354-49-4
1,2,2-tribromo-1,1,2-trifluoroethane
-
D
-
7783-61-1
silicon tetrafluoride
-
E
-
7783-42-8
thionyl fluoride
| Conditions | Yield |
|---|---|
| Irradiation (UV/VIS); irradiated (Hanovia S 500 lamp) in silica ampule, 20 h, further products; | A n/a B n/a C 49% D n/a E n/a |
-
-
16853-85-3
lithium aluminium tetrahydride
-
-
56144-86-6
SiF3SiHBr2
-
B
-
13465-71-9
trifluorosilane
-
C
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| React. occurs at room temp. (N2 or Ar, 15 min).; IR spectrum of volatile material indicates resulting compounds and 5% unreacted SiF3SiHBr2.; | A 5% B 45% C 45% |
-
-
13465-77-5
hexachlorodisilane
-
A
-
7647-01-0
hydrogenchloride
-
B
-
13830-68-7
disilicon hexafluoride
-
C
-
7783-61-1
silicon tetrafluoride
| Conditions | Yield |
|---|---|
| In 1,2-dichloro-ethane; acetonitrile Si2Cl6 dissolved in C2H4Cl2 added dropwise over 2 h to suspn. of KF in boiling MeCN, allowed to reflux for 30 min in slow stream of N2; gaseous products trapped in cooled (liq. N2) trap, analyzed by IR; | A n/a B 45% C n/a |
-
-
56144-86-6
SiF3SiHBr2
-
-
1191-15-7
i-Bu2AlH
-
A
-
13465-71-9
trifluorosilane
-
B
-
7783-61-1
silicon tetrafluoride
-
C
-
7440-21-3
monosilane
| Conditions | Yield |
|---|---|
| In carbon dioxide; isopropyl alcohol; toluene Condensing of Si-compd. at -196°C, warming to -78°C (2-propanol/CO2), addn. of i-Bu2AlH (toluene) in portions over 30 min (N2 or Ar), warming of mixt. (room temp., 15 min).; Removal of volatile compounds under vac., IR identification.; | A 40% B 20% C 40% |
-
-
56144-86-6
SiF3SiHBr2
-
-
22722-98-1
Na(1+)*AlH2(1+)*2OCH2CH2OCH3(1-)=NaAlH2(OCH2CH2OCH3)2
-
A
-
13465-71-9
trifluorosilane
-
B
-
7783-61-1
silicon tetrafluoride
-
C
-
7440-21-3
monosilane
| Conditions | Yield |
|---|---|
| In carbon dioxide; isopropyl alcohol; toluene Condensing of Si-compd. at -196°C, warming to -78°C (2-propanol/CO2), addn. of vitride (toluene) in portions over 30 min (N2 or Ar), warming of mixt. (room temp., 15 min).; Removal of volatile compounds under vac., IR identification.; | A 40% B 20% C 40% |
| Conditions | Yield |
|---|---|
| excess of SiF4, heating up to 400°C in a quartz tube; | 100% |
-
-
75-44-5
phosgene
-
-
7783-61-1
silicon tetrafluoride
-
A
-
353-50-4
Carbonyl fluoride
-
B
-
353-49-1
fluoroformyl chloride
| Conditions | Yield |
|---|---|
| In gaseous matrix molar ratio of educts 1:1, 400°C in a quartz tube; | A 0% B 100% |
-
-
420-60-0
trimethyltin fluoride
-
-
7783-61-1
silicon tetrafluoride
-
-
10569-17-2
tris(trimethylstannyl)phosphane
| Conditions | Yield |
|---|---|
| In tetrahydrofuran elem. anal., MAS; | A 100% B n/a |
| Conditions | Yield |
|---|---|
| In diethylene glycol dimethyl ether byproducts: CH4; SiF4 was bubbled through soln. of NaAlH4 in diglyme at atmospheric pressure, heated at 0-60°C in He; chromy.; elem. anal.; | 99% |
-
-
64-17-5
ethanol
-
-
7783-61-1
silicon tetrafluoride
-
-
7439-95-4
magnesium
-
B
-
78-10-4
tetraethoxy orthosilicate
| Conditions | Yield |
|---|---|
| Stage #1: ethanol; magnesium With iodine at 20℃; for 3.5h; Inert atmosphere; Reflux; Stage #2: silicon tetrafluoride for 2.5h; Inert atmosphere; Reflux; Stage #3: at 300℃; for 2h; Catalytic behavior; Reagent/catalyst; Temperature; Calcination; | A 98% B 82% |
-
-
67-56-1
methanol
-
-
7783-61-1
silicon tetrafluoride
-
-
7439-95-4
magnesium
-
B
-
681-84-5
tetramethylorthosilicate
| Conditions | Yield |
|---|---|
| Stage #1: methanol; magnesium With iodine at 20℃; for 1.5h; Inert atmosphere; Reflux; Stage #2: silicon tetrafluoride Inert atmosphere; Stage #3: at 300℃; for 2h; Catalytic behavior; Reagent/catalyst; Temperature; Calcination; | A 98% B 85% |
| Stage #1: methanol; magnesium at 20℃; for 3h; Stage #2: silicon tetrafluoride at 20℃; for 0.5h; Temperature; |
| Conditions | Yield |
|---|---|
| With CH3OH; NH3 In methanol introduction of NH3 into CH3OH in absence of air; introduction of SiF4;; filtration; distn. of the filtrate;; | A n/a B 95% |
| With methanol; ammonia In methanol introduction of NH3 into CH3OH in absence of air; introduction of SiF4;; filtration; distn. of the filtrate;; | A n/a B 95% |
| Conditions | Yield |
|---|---|
| With C2H5OH SiF4 and C2H5OH in presence of NH3;; | 92% |
| With ethanol SiF4 and C2H5OH in presence of NH3;; | 92% |
| Conditions | Yield |
|---|---|
| With hydrogen In neat (no solvent) in flow reactor at 180°C; the diluent used was H2; | 90% |
| In neat (no solvent) Kinetics; byproducts: CaF2; mech. activated in rotating flow-through reactor; rotation frequency 100-150 rpm, CaF2 heated at temp. of 180-190°C, SiF4+H2 (1/1 v/v) flow through; gaseous products frozen out with liq. N2; detd. by gas-chromy.; |
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