chlorine fluorosulfate
sulfur tetrafluoride
A
pentafluorosulfanyl chloride
B
trifluorosulfonium fluorosulfate
Conditions | Yield |
---|---|
In neat (no solvent) ClOSO2F trasferred under vac. to FEP reactor fitted with stainless-steel valve and held at -196°C, SF4 condensed, reactor placed in bath at -90°C and allowed to warm to -40°C for 4 h; reactor cooled to -70°C, volatile materials(SF5Cl) removed, reactor warmed to -40°C and then - to 23°C and held under dynamic vac. for 10 min; | A 77% B 38% |
sulfur
trichloroisocyanuric acid
A
fluorosulfonyl fluoride
B
pentafluorosulfanyl chloride
C
thionyl fluoride
Conditions | Yield |
---|---|
In acetonitrile at 20℃; Inert atmosphere; Darkness; Sealed tube; | A n/a B 47% C n/a |
chlorine trifluoride
sulfur tetrafluoride
pentafluorosulfanyl chloride
Conditions | Yield |
---|---|
In neat (no solvent) between 100 - 350°C under exclusion of water at 3 atm;; | |
In neat (no solvent) between 100 - 350°C under exclusion of water at 3 atm;; |
sulfur tetrafluoride
chlorine monofluoride
pentafluorosulfanyl chloride
Conditions | Yield |
---|---|
In neat (no solvent) at 100 - 300°C and 3 atm;; | |
In gaseous matrix Kinetics; Irradiation (UV/VIS); photochemical reaction (Ar laser, mean power 10 mW, 450-500 nm, 100 Torr xenon as buffer gas); not isolated; IR monitoring; | |
In neat (no solvent) at 100 - 300°C and 3 atm;; |
disulfur decafluoride
pentafluorosulfanyl chloride
Conditions | Yield |
---|---|
With chlorine In neat (no solvent) passing Cl2 and S2F10 through tube at 350°C;; | |
With chlorine In neat (no solvent) passing Cl2 and S2F10 through tube under reduced pressure;; | >99 |
disulfur dichloride
F5SNCl2
A
pentafluorosulfanyl chloride
B
SF5N=SCl2
Conditions | Yield |
---|---|
In further solvent(s) Cl2S2 is placed in a FEP-trap (dry-box), evacuated and cooled to -196°C, CFCl3 is condensed into trap, mixt. is warmed to room temp., into this mixt. Fe5SNCl2 is condensed (liquid N2), cooling to -100°C, mixt. is allowed to warm; mixt. is stirred under warming to -20°C for several hours, sepn.by fractional condensation in oil vac. in cold traps at -45, -50, -196°C, react. is followed by Raman-spectroscopy; |
dichlorodithionitronium hexafluoroarsenate
chlorine monofluoride
A
pentafluorosulfanyl chloride
B
{SF3}(1+)*{AsF6}(1-)=SF3AsF6
D
sulfur tetrafluoride
E
thionyl fluoride
Conditions | Yield |
---|---|
With fluorosulfonylchloride In not given SO2ClF and ClF were condensed onto (SCl)2NAsF6, mixt. was warmed to room temp. with srirring, 5 h; volatiles were removed, products were not isolated; products were analized by IR; | A n/a B n/a C 0% D n/a E <1 |
Conditions | Yield |
---|---|
With trifluoroacetic acid In acetonitrile at 20℃; for 14h; Inert atmosphere; |
pentafluorosulfanyl chloride
F5SNCl2
tris(pentafluorosulfanyl)amine
Conditions | Yield |
---|---|
In water at 20℃; under 1.50015 Torr; for 3.5h; UV-irradiation; | 94% |
pentafluorosulfanyl chloride
pentafuorosulfanyl hypochlorite
bis(pentafluorosulfur)oxide
Conditions | Yield |
---|---|
byproducts: SO2F2, SOF4, SF6; Irradiation (UV/VIS); irradn. for 4 h at 22°C; collection in a -196°C trap (dynamic vacuum); fractional condensation; SF5OSF5 and SF5O2SF5 in -111°C trap; mixt. heated in copper reactor at 237°C for 2.5 h;; fractional condensation yielded SF5OSF5 in a -118°C trap; further compounds (from decompn. of SF5O2SF5) in -196°C trap;; | 72% |
pentafluorosulfanyl chloride
N-Chlor-N-trifluormethyl-pentafluoraethylamin
N,N'-bis(perfluoroethyl)-N,N'-bis(trifluoromethyl)-hydrazine
Conditions | Yield |
---|---|
In gas Irradiation (UV/VIS); irradiation with PRK-2 lamp in silica flask at 20°C (45 h); | 70% |
In neat (no solvent, gas phase) Irradiation (UV/VIS); irradiation with PRK-2 lamp in silica flask at 20°C (45 h); | 70% |
heptafluorobutyronitrile
pentafluorosulfanyl chloride
sulfur pentafluoride (1-chloro-heptafluorobutylidene)amide
Conditions | Yield |
---|---|
Irradiation (UV/VIS); 20°C, 17.7 h; | 45% |
pentafluorosulfanyl chloride
N-Chlor-N-trifluormethyl-pentafluoraethylamin
sulfur pentafluoride pentafluoroethyl(trifluoromethyl)amide
Conditions | Yield |
---|---|
Irradiation (UV/VIS); in quartz flask, 20°C, 45 h, with PKR UV lamps; | 43% |
Irradiation (UV/VIS); in quartz flask, 20°C, 45 h, with PKR UV lamps; | 43% |
pentafluorosulfanyl chloride
trifluoroacetonitrile
sulfur pentafluoride (1-chloro-2,2,2-trifluoroethylidene)amide
Conditions | Yield |
---|---|
Irradiation (UV/VIS); 20°C, 14.5 h; | 32% |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: S2F10, (SF5)2NCl, Cl2; Irradiation (UV/VIS); SF5NCl2 and SF5Cl were loaded into a Pyrex flask to give a pressure of about 1 atm at room temp., mixt. was irradiated for 4.5 to 5 h with an internal medium-pressure Hg lamp; by-products included S2F10, Cl2, N2, and (SF5)2NCl; isolated by repeated trap-to-trap distn. of the volatile products (in the -30°C trap); elem. anal.; | 20% |
pentafluorosulfanyl chloride
sulfur dioxide
A
sulfuryl dichloride
B
fluorosulfonyl fluoride
C
disulfur decafluoride
D
pentafluorosulfur fluorosulfonate
E
thionyl fluoride
Conditions | Yield |
---|---|
byproducts: SiF4; other Radiation; photochemical reaction with 253.7 nm radiation, 48 h, in glass vessel; | A n/a B n/a C <1 D n/a E n/a |
Conditions | Yield |
---|---|
In not given byproducts: SF4; react. of P with SF5Cl;; | |
In not given byproducts: SF4; react. of P with SF5Cl;; |
chloro-trimethyl-silane
pentafluorosulfanyl chloride
sulfur dichloride
Conditions | Yield |
---|---|
byproducts: Cl2, (CH3)3SiF; a mixt. of SF5Cl and (CH3)3SiCl is held at 0°C for 2 h; distn.; |
pentafluorosulfanyl chloride
A
Carbonyl fluoride
B
fluoroformyl chloride
C
sulfur tetrafluoride
D
sulfur(VI) hexafluoride
Conditions | Yield |
---|---|
With carbon monoxide byproducts: S2F10, COS, SO2F2; Irradiation (UV/VIS); |
pentafluorosulfanyl chloride
A
FCl(1-)
B
SF5Cl(1-)
D
chloride
Conditions | Yield |
---|---|
In gas other Radiation; electron attachment by SF5Cl in the energy range 0-20 eV studied in a beam experiment at room temp.; only a weak signal of SF5Cl(1-) is observed; |
pentafluorosulfanyl chloride
disulfur decafluoride
Conditions | Yield |
---|---|
With hydrogen In neat (no solvent) other Radiation; photochemical reduction;; | |
In neat (no solvent) |
pentafluorosulfanyl chloride
tetrakis(dimethylamido)diborane
boron trichloride
Conditions | Yield |
---|---|
byproducts: Cl2, SF4; excess SF5Cl; | |
byproducts: Cl2, SF4; excess SF5Cl; |
pentafluorosulfanyl chloride
Lithium; 2,3,4,5,6-pentafluoro-benzenethiolate
A
bis(pentafluorophenyl) disulfide
B
bis(pentafluorophenyl)trisulfane
pentafluorosulfanyl chloride
Li(1+)*CF3S(1-)=LiSCF3
bis(trifluoromethyl)trisulfide
pentafluorosulfanyl chloride
Li(1+)*CF3S(1-)=LiSCF3
Bis(trifluoromethyl)disulfid
Conditions | Yield |
---|---|
In diethyl ether -78°C, among other products; | |
In diethyl ether -78°C, among other products; |
pentafluorosulfanyl chloride
bis(pentafluorosulfur)oxide
Conditions | Yield |
---|---|
With oxygen In neat (no solvent) Irradiation (UV/VIS); photochemical oxidation;; | |
With oxygen In neat (no solvent) Irradiation (UV/VIS); photochemical oxidation;; |
pentafluorosulfanyl chloride
bis(pentafluorosulfur) peroxide
Conditions | Yield |
---|---|
With oxygen In neat (no solvent) Irradiation (UV/VIS); photochemical oxidation;; | |
With oxygen In neat (no solvent) Irradiation (UV/VIS); photochemical oxidation;; |
pentafluorosulfanyl chloride
Chlorotrifluoroethylene
(2,2-dichlorotrifluoroethyl)pentafluorosulfur(VI)
Conditions | Yield |
---|---|
In trichlorofluoromethane 100°C , 10 h; | |
90°C , 10 h ,in presence of dibenzoylperoxide; | |
In trichlorofluoromethane 100°C , 10 h; | |
90°C , 10 h ,in presence of dibenzoylperoxide; |
pentafluorosulfanyl chloride
Chlorotrifluoroethylene
(1,2-dichlorotrifluoroethyl)pentafluorosulfur(VI)
Conditions | Yield |
---|---|
Irradiation (UV/VIS); 5 h; | |
Irradiation (UV/VIS); 5 h; |
pentafluorosulfanyl chloride
N-chlorobistrifluoromethylamine
sulfur pentafluoride bis(trifluoromethylamide)
Conditions | Yield |
---|---|
Irradiation (UV/VIS); irradiation 44 h and heating to 200°C, 2 h; | |
Irradiation (UV/VIS); irradiation 44 h and heating to 200°C, 2 h; |
pentafluorosulfanyl chloride
pentafluorophenyl lithium
bis(pentafluorophenyl) sulfoxide
Conditions | Yield |
---|---|
In diethyl ether -78°C, 5 h; | 50-60 |
pentafluorosulfanyl chloride
lithium S,S-bis(trifluoromethyl)sulfimide
bis-(trifluoromethyl)sulfide
Conditions | Yield |
---|---|
byproducts: LiCl; educts condensed at -196°C, followed by warming to room temp., decomposition products formed, too; | |
byproducts: LiCl; educts condensed at -196°C, followed by warming to room temp., decomposition products formed, too; |
pentafluorosulfanyl chloride
Lithium; 2,3,4,5,6-pentafluoro-benzenethiolate
A
pentafluorobenzenesulfenyl chloride
B
bis(pentafluorophenyl) disulfide
C
bis(pentafluorophenyl)trisulfane
Conditions | Yield |
---|---|
In diethyl ether molar ratio 3 : 1 to 4 : 1, -78.degre; | |
In diethyl ether molar ratio 3 : 1 to 4 : 1, -78.degre; |
Product Name: Sulphur chloropentafluoride
Synonyms:Chloropentafluorosulfur ; Monochloropentafluorosulfur ; Pentafluorosulfurchloride ; SClF5 ; SF5Cl ; Silfur chloropentafluoride ; Sulfur chloride fluoride ; Sulfur chloride fluoride (SClF5).
CAS: 13780-57-9
Molecular Formula of Sulphur chloropentafluoride (13780-57-9) : ClF5S
Molecular Weight of Sulphur chloropentafluoride (13780-57-9) : 162.51
Molecular Struture of Sulphur chloropentafluoride (13780-57-9) :
EINECS: 237-431-0
Product Categories:
Mol File: 13780-57-9.mol
Melting point: -64°C
Boiling point: -21°C
1. | ihl-rat LCLo:100 ppm/1H | BJIMAG British Journal of Industrial Medicine. 27 (1970),1. |
Hazard Codes T
Risk Statements 23-34
23: Toxic by inhalation
34: Sulphur chloropentafluoride (13780-57-9) causes burns
Safety Statements 26-36/37/39-45
26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
45: In case of accident or if you feel unwell, seek medical advice immediately (show label where possible)
36/37/39: Wear suitable protective clothing, gloves and eye/face protection
RIDADR 3308
Hazard Note Toxic
OSHA PEL: TWA 2.5 mg(F)/m3
ACGIH TLV: TWA 2.5 mg(F)/m3; BEI: 3 mg/g creatinine of fluorides in urine prior to shift; 10 mg/g creatinine of fluorides in urine at end of shift.
NIOSH REL: (Inorganic Fluorides) TWA 2.5 mg(F)/m3
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