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13780-57-9

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13780-57-9 Usage

General Description

Sulphur chloropentafluoride is a chemical compound with the formula SCl5F. It is a colorless gas at room temperature and is highly reactive with water and air. Sulphur chloropentafluoride is primarily used as a precursor in the synthesis of various fluorine-containing compounds, particularly in organic chemistry and in the production of high-performance polymers. It is also used as a fluorinating agent in the pharmaceutical industry for the synthesis of fluorinated drugs. Sulphur chloropentafluoride has stringent safety precautions due to its highly reactive and toxic nature, and it must be handled and stored with care.

Check Digit Verification of cas no

The CAS Registry Mumber 13780-57-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,8 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13780-57:
(7*1)+(6*3)+(5*7)+(4*8)+(3*0)+(2*5)+(1*7)=109
109 % 10 = 9
So 13780-57-9 is a valid CAS Registry Number.
InChI:InChI=1/ClF5S/c1-7(2,3,4,5)6

13780-57-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name chloro(pentafluoro)-λ<sup>6</sup>-sulfane

1.2 Other means of identification

Product number -
Other names Sulfur monochloride pentafluoride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13780-57-9 SDS

13780-57-9Synthetic route

chlorine fluorosulfate
13997-90-5

chlorine fluorosulfate

sulfur tetrafluoride
7783-60-0

sulfur tetrafluoride

A

pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

B

trifluorosulfonium fluorosulfate
88548-61-2

trifluorosulfonium fluorosulfate

Conditions
ConditionsYield
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
10544-50-0

sulfur

potassium fluoride

potassium fluoride

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

A

fluorosulfonyl fluoride
640723-20-2, 2699-79-8, 12769-73-2

fluorosulfonyl fluoride

B

pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

C

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
In acetonitrile at 20℃; Inert atmosphere; Darkness; Sealed tube;A n/a
B 47%
C n/a
chlorine trifluoride
7790-91-2

chlorine trifluoride

sulfur tetrafluoride
7783-60-0

sulfur tetrafluoride

pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

Conditions
ConditionsYield
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
7783-60-0

sulfur tetrafluoride

chlorine monofluoride
7790-89-8

chlorine monofluoride

pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

Conditions
ConditionsYield
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
5714-22-7

disulfur decafluoride

pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

Conditions
ConditionsYield
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
10025-67-9

disulfur dichloride

F5SNCl2
22650-46-0

F5SNCl2

A

pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

B

SF5N=SCl2
25502-15-2

SF5N=SCl2

Conditions
ConditionsYield
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
60563-08-8

dichlorodithionitronium hexafluoroarsenate

chlorine monofluoride
7790-89-8

chlorine monofluoride

A

pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

B

{SF3}(1+)*{AsF6}(1-)=SF3AsF6
30313-36-1

{SF3}(1+)*{AsF6}(1-)=SF3AsF6

C

difluoro-dithionitronium hexafluoroarsenate(V)

difluoro-dithionitronium hexafluoroarsenate(V)

D

sulfur tetrafluoride
7783-60-0

sulfur tetrafluoride

E

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
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
potassium fluoride

potassium fluoride

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

sulfur
7704-34-9

sulfur

pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

Conditions
ConditionsYield
With trifluoroacetic acid In acetonitrile at 20℃; for 14h; Inert atmosphere;
pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

F5SNCl2
22650-46-0

F5SNCl2

tris(pentafluorosulfanyl)amine
100312-09-2

tris(pentafluorosulfanyl)amine

Conditions
ConditionsYield
In water at 20℃; under 1.50015 Torr; for 3.5h; UV-irradiation;94%
pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

pentafuorosulfanyl hypochlorite
22675-70-3

pentafuorosulfanyl hypochlorite

bis(pentafluorosulfur)oxide
42310-84-9

bis(pentafluorosulfur)oxide

Conditions
ConditionsYield
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
13780-57-9

pentafluorosulfanyl chloride

N-Chlor-N-trifluormethyl-pentafluoraethylamin
25246-37-1

N-Chlor-N-trifluormethyl-pentafluoraethylamin

N,N'-bis(perfluoroethyl)-N,N'-bis(trifluoromethyl)-hydrazine
25246-38-2

N,N'-bis(perfluoroethyl)-N,N'-bis(trifluoromethyl)-hydrazine

Conditions
ConditionsYield
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
375-00-8

heptafluorobutyronitrile

pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

sulfur pentafluoride (1-chloro-heptafluorobutylidene)amide
2261-34-9

sulfur pentafluoride (1-chloro-heptafluorobutylidene)amide

Conditions
ConditionsYield
Irradiation (UV/VIS); 20°C, 17.7 h;45%
pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

N-Chlor-N-trifluormethyl-pentafluoraethylamin
25246-37-1

N-Chlor-N-trifluormethyl-pentafluoraethylamin

sulfur pentafluoride pentafluoroethyl(trifluoromethyl)amide
26981-28-2

sulfur pentafluoride pentafluoroethyl(trifluoromethyl)amide

Conditions
ConditionsYield
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
13780-57-9

pentafluorosulfanyl chloride

trifluoroacetonitrile
353-85-5

trifluoroacetonitrile

sulfur pentafluoride (1-chloro-2,2,2-trifluoroethylidene)amide
2375-40-8

sulfur pentafluoride (1-chloro-2,2,2-trifluoroethylidene)amide

Conditions
ConditionsYield
Irradiation (UV/VIS); 20°C, 14.5 h;32%
pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

F5SNCl2
22650-46-0

F5SNCl2

tetrakis(pentafluorosulfanyl)hydrazine

tetrakis(pentafluorosulfanyl)hydrazine

Conditions
ConditionsYield
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
13780-57-9

pentafluorosulfanyl chloride

sulfur dioxide
7446-09-5

sulfur dioxide

A

sulfuryl dichloride
7791-25-5

sulfuryl dichloride

B

fluorosulfonyl fluoride
640723-20-2, 2699-79-8, 12769-73-2

fluorosulfonyl fluoride

C

disulfur decafluoride
5714-22-7

disulfur decafluoride

D

pentafluorosulfur fluorosulfonate
81439-35-2

pentafluorosulfur fluorosulfonate

E

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
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
phosphorus

phosphorus

pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

phosphorus pentafluoride
7647-19-0, 874483-74-6

phosphorus pentafluoride

Conditions
ConditionsYield
In not given byproducts: SF4; react. of P with SF5Cl;;
In not given byproducts: SF4; react. of P with SF5Cl;;
chloro-trimethyl-silane
75-77-4

chloro-trimethyl-silane

pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

sulfur dichloride
10545-99-0

sulfur dichloride

Conditions
ConditionsYield
byproducts: Cl2, (CH3)3SiF; a mixt. of SF5Cl and (CH3)3SiCl is held at 0°C for 2 h; distn.;
pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

A

Carbonyl fluoride
353-50-4

Carbonyl fluoride

B

fluoroformyl chloride
353-49-1

fluoroformyl chloride

C

sulfur tetrafluoride
7783-60-0

sulfur tetrafluoride

D

sulfur(VI) hexafluoride
2551-62-4

sulfur(VI) hexafluoride

Conditions
ConditionsYield
With carbon monoxide byproducts: S2F10, COS, SO2F2; Irradiation (UV/VIS);
pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

A

FCl(1-)
807261-54-7

FCl(1-)

B

SF5Cl(1-)
141248-49-9

SF5Cl(1-)

C

fluoride

fluoride

D

chloride
16887-00-6

chloride

E

F5S(1-)

F5S(1-)

Conditions
ConditionsYield
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
13780-57-9

pentafluorosulfanyl chloride

disulfur decafluoride
5714-22-7

disulfur decafluoride

Conditions
ConditionsYield
With hydrogen In neat (no solvent) other Radiation; photochemical reduction;;
In neat (no solvent)
pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

tetrakis(dimethylamido)diborane
1630-79-1

tetrakis(dimethylamido)diborane

boron trichloride
10294-34-5

boron trichloride

Conditions
ConditionsYield
byproducts: Cl2, SF4; excess SF5Cl;
byproducts: Cl2, SF4; excess SF5Cl;
pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

Lithium; 2,3,4,5,6-pentafluoro-benzenethiolate
40779-99-5

Lithium; 2,3,4,5,6-pentafluoro-benzenethiolate

A

bis(pentafluorophenyl) disulfide
1494-06-0

bis(pentafluorophenyl) disulfide

B

bis(pentafluorophenyl)trisulfane
52082-75-4

bis(pentafluorophenyl)trisulfane

pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

Li(1+)*CF3S(1-)=LiSCF3
65844-06-6

Li(1+)*CF3S(1-)=LiSCF3

bis(trifluoromethyl)trisulfide
372-06-5

bis(trifluoromethyl)trisulfide

pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

Li(1+)*CF3S(1-)=LiSCF3
65844-06-6

Li(1+)*CF3S(1-)=LiSCF3

Bis(trifluoromethyl)disulfid
372-64-5

Bis(trifluoromethyl)disulfid

Conditions
ConditionsYield
In diethyl ether -78°C, among other products;
In diethyl ether -78°C, among other products;
pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

bis(pentafluorosulfur)oxide
42310-84-9

bis(pentafluorosulfur)oxide

Conditions
ConditionsYield
With oxygen In neat (no solvent) Irradiation (UV/VIS); photochemical oxidation;;
With oxygen In neat (no solvent) Irradiation (UV/VIS); photochemical oxidation;;
pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

bis(pentafluorosulfur) peroxide
12395-41-4

bis(pentafluorosulfur) peroxide

Conditions
ConditionsYield
With oxygen In neat (no solvent) Irradiation (UV/VIS); photochemical oxidation;;
With oxygen In neat (no solvent) Irradiation (UV/VIS); photochemical oxidation;;
pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

Chlorotrifluoroethylene
79-38-9

Chlorotrifluoroethylene

(2,2-dichlorotrifluoroethyl)pentafluorosulfur(VI)
3830-75-9

(2,2-dichlorotrifluoroethyl)pentafluorosulfur(VI)

Conditions
ConditionsYield
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
13780-57-9

pentafluorosulfanyl chloride

Chlorotrifluoroethylene
79-38-9

Chlorotrifluoroethylene

(1,2-dichlorotrifluoroethyl)pentafluorosulfur(VI)
22687-89-4

(1,2-dichlorotrifluoroethyl)pentafluorosulfur(VI)

Conditions
ConditionsYield
Irradiation (UV/VIS); 5 h;
Irradiation (UV/VIS); 5 h;
pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

N-chlorobistrifluoromethylamine
431-94-7

N-chlorobistrifluoromethylamine

sulfur pentafluoride bis(trifluoromethylamide)
13888-13-6

sulfur pentafluoride bis(trifluoromethylamide)

Conditions
ConditionsYield
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
13780-57-9

pentafluorosulfanyl chloride

pentafluorophenyl lithium
1076-44-4

pentafluorophenyl lithium

bis(pentafluorophenyl) sulfoxide
26346-84-9

bis(pentafluorophenyl) sulfoxide

Conditions
ConditionsYield
In diethyl ether -78°C, 5 h;50-60
pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

lithium S,S-bis(trifluoromethyl)sulfimide
61097-18-5

lithium S,S-bis(trifluoromethyl)sulfimide

bis-(trifluoromethyl)sulfide
371-78-8

bis-(trifluoromethyl)sulfide

Conditions
ConditionsYield
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
13780-57-9

pentafluorosulfanyl chloride

Lithium; 2,3,4,5,6-pentafluoro-benzenethiolate
40779-99-5

Lithium; 2,3,4,5,6-pentafluoro-benzenethiolate

A

pentafluorobenzenesulfenyl chloride
27918-31-6

pentafluorobenzenesulfenyl chloride

B

bis(pentafluorophenyl) disulfide
1494-06-0

bis(pentafluorophenyl) disulfide

C

bis(pentafluorophenyl)trisulfane
52082-75-4

bis(pentafluorophenyl)trisulfane

Conditions
ConditionsYield
In diethyl ether molar ratio 3 : 1 to 4 : 1, -78.degre;
In diethyl ether molar ratio 3 : 1 to 4 : 1, -78.degre;

13780-57-9Relevant articles and documents

Photochemistry of the chlorine monofluoride, CIF. Thermal and photochemical reactions with sulfur tetrafluoride SF4

Naulin, Christian,Bougon, Roland

, p. 2155 - 2158 (1980)

The thermal and photochemical reactions of chlorine monofluoride have been studied with xenon, perfluoroethane C2F6, and sulfur tetrafluoride, SF4, which had been considered as possible scavengers for the excited or unstable species.No reaction has been observed with Xe and C2F6 either under thermal or photochemical activation.Photochemical reaction of CIF with SF4 has been studied at several wavelengths with a cw laser.From these studies, two reaction paths have been emphasized: (1) the molecular addition of ClF* to SF4 to give sulfur chloropentafluoride SF5Cland (2) a typical laser induced radical process yielding disulfur decafluoride S2F10 and chloride Cl2.This former effect has been shown to be hidden at low mean power irradiation by the thermal reaction which seems to be dramatically enhanced at low pressure by wall-catalyzed processes.

METHOD FOR PREPARING A POLYFLUORINATED COMPOUND

-

Page/Page column 50-51, (2019/12/25)

The present invention relates to a process for preparing a polyfluorinated compound of formula Ar-Ri(l), wherein Ar-Ri(l) is an aromatic ring system wherein R1 is selected from the group consisting of SF4CI, SF3, SF2CF3, TeFS, TeF4CF3, SeF3, IF2, SeF2CF3, and IF4, X2 is N or CR2, X3 is N or CR 3, X 4 is N or CR 4, X 5 is N or CR 5, X 6 is N or CR 6, and the total number of nitrogen atoms in the aromatic ring system is between 0 and 3, and if X 5 is CR 5 and X 6 is CR 6 R 5 and R 6 may form together a saturated or unsaturated five or six membered ring system comprising one or more nitrogen, wherein said five or six membered ring system may be substituted with one or more residues R 7 said process involving the following reaction step reacting a starting material selected from the group consisting of Ar2S2, Ar2Te2, Ar2Se2, ArSCF3, Arl, ArTeCF3, ArSeCF3, ArSCF3, and ArSCI, wherein Ar has the same definition as above, with trichloroisocyanuric acid (TCICA) of the formula (III) in the presence of the alkali metal fluoride (MF).

The Reaction of S2NAsF6 with Halogens: Preparation and X-Ray Crystal Structure of Bis(difluorothio)nitronium Hexafluoroarsenate(V), (SF2)2NAsF6; Preparation of (SBr)2NAsF6, and Vibrational Spectrum and Normal-co-ordinate Analysis of the (SX)2N+ (X=Cl or Br) Cations

Brooks, Wendell V. F.,MacLean, Gregory K.,Passmore, Jack,White, Peter S.,Wong, Chi-Ming

, p. 1961 - 1968 (2007/10/02)

Solutions of S2NAsF6 in liquid SO2 react with elemental chlorine and bromine yielding (SX)2NAsF6 (X=Cl or Br), essentially quantitatively.No reaction was detected with iodine.The vibrational spectrum of (SBr)2N+ was similar to that of (SCl)2N+ of known structure, implying a similar structure for the bromine derivative.This conclusion was supported by a normal-co-ordinate analysis of (SX)2N+.The analysis was consistent with some positive interaction between the halogen atoms in (SX)2N+, possibly accounting for the cis planar geometry of these cations.Attempts to prepare (SF)2NAsF6 were unsuccessful.However, (SF2)2NAsF6 was synthesised by the reaction of S2NAsF6 and XeF2 in liquid SO2F2, essentially quantitatively.The structure of (SF2)2NAsF6 was determined by X-ray diffraction.The crystals are orthorhombic with a=14.909(1), b=9.843(4), c=12.113(1) Angstroem, and Z=8.The structure was refined in space group Pbca to a conventional R factor of 0.076 for 902 independent reflections with I>2?(I).It consists of discrete (SF2)2N+ and AsF6- with some cation-anion interactions.The (SF2)2N+ cation has approximate C2γ symmetry with essentially eclipsed fluorine-sulphur bonds as viewed along the sulphur-sulphur axis.The average S-N and S-F distances are 1.551(10) and 1.523(8) Angstroem, and the average FSF and FSN bond angles are 94.0(5) and 100.2(6) deg.The SNS bond angle is 121.1(6) deg.The vibrational spectrum of (SF2)2NAsF6 is reported.

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