Product Name

  • Name

    TRIFLUOROMETHYLSULPHENYL CHLORIDE

  • EINECS
  • CAS No. 421-17-0
  • Article Data57
  • CAS DataBase
  • Density 1.573g/cm3
  • Solubility
  • Melting Point
  • Formula CCl F3 S
  • Boiling Point °Cat760mmHg
  • Molecular Weight 136.525
  • Flash Point °C
  • Transport Information
  • Appearance
  • Safety Explosive reaction with chlorine fluorides. When heated to decomposition it emits toxic fumes of F, Cl, and SOx. See also FLUORIDES.
  • Risk Codes 26-34
  • Molecular Structure Molecular Structure of 421-17-0 (TRIFLUOROMETHYLSULPHENYL CHLORIDE)
  • Hazard Symbols
  • Synonyms Perfluoromethylsulfenylchloride; Trifluoromethanesulfenyl chloride; Trifluoromethylsulfenyl chloride;Trifluoromethylsulphenyl chloride
  • PSA 25.30000
  • LogP 2.39320

Synthetic route

hydrogen fluoride
7664-39-3

hydrogen fluoride

chlorothio-trichloro-methane
594-42-3

chlorothio-trichloro-methane

A

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

B

Bis(trifluoromethyl)disulfid
372-64-5

Bis(trifluoromethyl)disulfid

C

Trifluoro-methanethiosulfonic acid S-trifluoromethyl ester
358-15-6

Trifluoro-methanethiosulfonic acid S-trifluoromethyl ester

Conditions
ConditionsYield
180°C; chrom oxide fluoride catalyst;A 74%
B n/a
C n/a
sodium fluoride

sodium fluoride

chlorothio-trichloro-methane
594-42-3

chlorothio-trichloro-methane

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

Conditions
ConditionsYield
In further solvent(s) in tetramethylsulphone at 170-250°C;47%
In acetonitrile 170-250°C;47%
In acetonitrile 170-250°C;47%
In further solvent(s) in tetramethylsulphone at 170-250°C;47%
In acetonitrile 170-250°C;47%
potassium fluoride

potassium fluoride

chlorodifluoromethansulfenylchloride
993-38-4

chlorodifluoromethansulfenylchloride

A

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

B

chlorodifluoromethanesulphenic acid fluoride
17742-03-9

chlorodifluoromethanesulphenic acid fluoride

Conditions
ConditionsYield
at 150°C;A 25%
B 5%
at 150°C;A 25%
B 5%
chlorodifluoromethansulfenylchloride
993-38-4

chlorodifluoromethansulfenylchloride

antimony(III) fluoride
7783-56-4

antimony(III) fluoride

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

Conditions
ConditionsYield
11%
11%
chlorodifluoromethansulfenylchloride
993-38-4

chlorodifluoromethansulfenylchloride

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

Conditions
ConditionsYield
With antimonypentachloride; antimony(III) fluoride
Bis(trifluoromethyl)disulfid
372-64-5

Bis(trifluoromethyl)disulfid

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

Conditions
ConditionsYield
With chlorine Irradiation.bei mehrtaegiger Bestrahlung mit UV-Licht;
With chlorine Irradiation (UV/VIS);
With chlorine Irradiation (UV/VIS);
1,1,1-trifluoromethanesulfenylamine
1512-33-0

1,1,1-trifluoromethanesulfenylamine

A

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

B

S2Cl2, Cl3S3N3

S2Cl2, Cl3S3N3

Conditions
ConditionsYield
With chlorine at -30℃; for 0.5h; Product distribution;
thiocarbonyl fluoride
420-32-6

thiocarbonyl fluoride

chlorine monofluoride
7790-89-8

chlorine monofluoride

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

sodium fluoride

sodium fluoride

chlorothio-trichloro-methane
594-42-3

chlorothio-trichloro-methane

A

chlorodifluoromethansulfenylchloride
993-38-4

chlorodifluoromethansulfenylchloride

B

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

CF3SCNCFSSCF3

CF3SCNCFSSCF3

A

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

B

trifluoromethylcarbamoyldisulfane
33278-65-8

trifluoromethylcarbamoyldisulfane

Conditions
ConditionsYield
With hydrogenchloride; water byproducts: HF;
With HCl; H2O byproducts: HF;
Methanesulfenyl chloride
5813-48-9

Methanesulfenyl chloride

trifluoromethylsulfenyl fluoride
17742-04-0

trifluoromethylsulfenyl fluoride

A

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

B

trifluoromethyl disulphide
14410-21-0

trifluoromethyl disulphide

C

Methylsulfur trifluoride
65082-47-5

Methylsulfur trifluoride

Conditions
ConditionsYield
-50°C;
-50°C;
1,1,1-trifluoromethanesulfenylamine
1512-33-0

1,1,1-trifluoromethanesulfenylamine

A

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

B

ammonium chloride

ammonium chloride

Conditions
ConditionsYield
With hydrogenchloride
With HCl
trifluoromethylmercaptoisocyanate
691-03-2

trifluoromethylmercaptoisocyanate

bis(trifluoromethylthio) amine
763-24-6

bis(trifluoromethylthio) amine

dichlorofluoromethanesulphenyl chloride
2712-93-8

dichlorofluoromethanesulphenyl chloride

A

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

B

trifluoromethylmercapto-bis(dichlorofluoromethylmercapto)amine
34153-27-0

trifluoromethylmercapto-bis(dichlorofluoromethylmercapto)amine

C

trimethylamine hydrochloride
593-81-7

trimethylamine hydrochloride

chlorodifluoromethanesulphenic acid fluoride
17742-03-9

chlorodifluoromethanesulphenic acid fluoride

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

Conditions
ConditionsYield
room temp.;
chlorodifluoromethansulfenylchloride
993-38-4

chlorodifluoromethansulfenylchloride

trifluoromethylmercaptoisocyanate
691-03-2

trifluoromethylmercaptoisocyanate

bis(trifluoromethylthio) amine
763-24-6

bis(trifluoromethylthio) amine

A

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

B

trifluoromethylmercapto-bis(chlorodifluoromethylmercapto)amine
34153-25-8

trifluoromethylmercapto-bis(chlorodifluoromethylmercapto)amine

C

trimethylamine hydrochloride
593-81-7

trimethylamine hydrochloride

chlorothio-trichloro-methane
594-42-3

chlorothio-trichloro-methane

A

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

B

Bis(trifluoromethyl)disulfid
372-64-5

Bis(trifluoromethyl)disulfid

C

trifluoromethanesulfinyl fluoride
812-12-4

trifluoromethanesulfinyl fluoride

Conditions
ConditionsYield
fluorination;
fluorination;
trifluoromethylmercapto carbamic acid chloride
6080-81-5

trifluoromethylmercapto carbamic acid chloride

A

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

B

14,14,14-Trifluor-13-thia-2,4,6,8,10,12-hexaaza-tetradecan-pentaon-(3,5,7,9,11)-saeurechlorid
6417-75-0

14,14,14-Trifluor-13-thia-2,4,6,8,10,12-hexaaza-tetradecan-pentaon-(3,5,7,9,11)-saeurechlorid

Conditions
ConditionsYield
20°C;
20°C;
N-Chlor-bis(fluorcarbonyl)-amin
42016-33-1

N-Chlor-bis(fluorcarbonyl)-amin

mercury bis(trifluoromethanethiolate)
21259-75-6

mercury bis(trifluoromethanethiolate)

A

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

B

Hg(2+)*(FCO)2N(1-)*SCF3(1-)=(FCO)2NHgSCF3

Hg(2+)*(FCO)2N(1-)*SCF3(1-)=(FCO)2NHgSCF3

mercury bis(trifluoromethanethiolate)
21259-75-6

mercury bis(trifluoromethanethiolate)

chlorine
7782-50-5

chlorine

A

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

B

Bis(trifluoromethyl)disulfid
372-64-5

Bis(trifluoromethyl)disulfid

C

trifluoromethylthio-mercury(II) chloride

trifluoromethylthio-mercury(II) chloride

Conditions
ConditionsYield
-22°C;
N,N'-bis(trifluoromethylmercapto)-chloroformamidine
36668-60-7

N,N'-bis(trifluoromethylmercapto)-chloroformamidine

N,N,N'-tris(trifluoromethylmercapto)-chloroformamidine
36668-61-8

N,N,N'-tris(trifluoromethylmercapto)-chloroformamidine

A

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

B

(CF3S)2NCN

(CF3S)2NCN

C

hexakis(trifluoromethylmercapto)melamine
36757-19-4

hexakis(trifluoromethylmercapto)melamine

Conditions
ConditionsYield
With trimethylamineA n/a
B 0%
C n/a
With (CH3)3NA n/a
B 0%
C n/a
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

hypofluorous acid trifluoromethyl ester
373-91-1

hypofluorous acid trifluoromethyl ester

trifluoro(trifluoromethyl)sulfur(IV)
374-10-7

trifluoro(trifluoromethyl)sulfur(IV)

Conditions
ConditionsYield
at -78°C, 0.5 h;100%
at -78°C, 0.5 h;100%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

N-chlorobistrifluoromethylketimine
10181-78-9

N-chlorobistrifluoromethylketimine

trifuloromethylsulfur perfluoroisopropylideneamide
31340-34-8

trifuloromethylsulfur perfluoroisopropylideneamide

Conditions
ConditionsYield
With mercury in Carius tube;100%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

water
7732-18-5

water

chlorine
7782-50-5

chlorine

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
excess of Cl2 and H2O, 20°C, 7 days;98%
excess of Cl2 and H2O, 20°C, 7 days;98%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

bis(sulfinylamido)tellurane
124824-09-5

bis(sulfinylamido)tellurane

bis(sulfinylamido) tellurium(IV) chloride
160785-74-0

bis(sulfinylamido) tellurium(IV) chloride

Conditions
ConditionsYield
In dichloromethane byproducts: CF3SSCF3; 2 equiv. of CF3SCl was condensed to Te-compd., stirred for 12 h at -60 ° C; volatiles were removed in vac., solid was dried in vac. for 12 h at 20 °C.;97%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

ethyl acetate
141-78-6

ethyl acetate

ethyl esetrs of α-(trifluoromethylthio)acetic acid
42105-37-3

ethyl esetrs of α-(trifluoromethylthio)acetic acid

Conditions
ConditionsYield
-20 to +24°C;96%
-20 to +24°C;96%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

bis(sulfinylamido) tellurium(IV) chloride
160785-74-0

bis(sulfinylamido) tellurium(IV) chloride

Te2Cl5N

Te2Cl5N

Conditions
ConditionsYield
In dichloromethane byproducts: SO2, CF3SSCF3; Te-compd. and CF3SCl in 1:2 molar ratio were stirred for 12 h at 22 ° C; volatiles were detected by IR;96%
In dichloromethane byproducts: SO2, CF3SNSO; 1 equiv. of CF3SCl was condensed to Te-compd., stirred for 3 d at -15 ° C; volatiles were identified by GC-MS and (19)F NMR;95%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

cyclohexene
110-83-8

cyclohexene

rac-(1R,2R)-1-chloro-2-[(trifluoromethyl)sulfanyl]cyclohexane

rac-(1R,2R)-1-chloro-2-[(trifluoromethyl)sulfanyl]cyclohexane

Conditions
ConditionsYield
trifluoroacetic acid at -20℃;95%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

bis(trifluoromethylthio)tellurium
83665-28-5

bis(trifluoromethylthio)tellurium

Conditions
ConditionsYield
With bis(triphenylstannyl)tellurium In various solvent(s) at 20℃; for 4h;95%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

chlorine trifluoride
7790-91-2

chlorine trifluoride

trifluoro(trifluoromethyl)sulfur(IV)
374-10-7

trifluoro(trifluoromethyl)sulfur(IV)

Conditions
ConditionsYield
In dichloromethane -78°C;95%
In dichloromethane -78°C;95%
In further solvent(s) in CF2Cl2 at -196 to -78°C;
In further solvent(s) in CF2Cl2 at -196 to -78°C;
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

trifluoromethylsulfinyl chloride
20621-29-8

trifluoromethylsulfinyl chloride

Conditions
ConditionsYield
With m-chloroperbenzoic acid oxidn., from -20 to +25°C, 12 h;95%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

Trifluormethylselenosilber
75264-94-7

Trifluormethylselenosilber

trifluoromethyl trifluoromethanesulfenoselenoate
73076-98-9

trifluoromethyl trifluoromethanesulfenoselenoate

Conditions
ConditionsYield
at -60℃;93%
-60°C;93-94
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

β-aminocinnamic amide
23787-16-8

β-aminocinnamic amide

β-amino-α-trifluoromethylthio-cinnamic acid amide

β-amino-α-trifluoromethylthio-cinnamic acid amide

Conditions
ConditionsYield
In chloroform Heating; 0 deg C, 30 min, room temperature, 20 h;90%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

β-imino-β-phenylpropionitrile
16187-90-9

β-imino-β-phenylpropionitrile

β-amino-α-trifluoromethylthio-cinnamic acid nitrile

β-amino-α-trifluoromethylthio-cinnamic acid nitrile

Conditions
ConditionsYield
In chloroform Heating; 0 deg C, 30 min, room temperature, 20 h;90%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

1,2-Dichloroethylene
540-59-0

1,2-Dichloroethylene

Trifluormethyl-1,2,2-trichlorethyl-sulfid
40302-61-2

Trifluormethyl-1,2,2-trichlorethyl-sulfid

Conditions
ConditionsYield
Irradiation (UV/VIS); 3:2 cis-trans isomer 1,2-dichloroethylene; distn.;90%
Irradiation (UV/VIS); 3:2 cis-trans isomer 1,2-dichloroethylene; distn.;90%
80%
80%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

silver fluoride

silver fluoride

A

trifluoromethylsulfenyl fluoride
17742-04-0

trifluoromethylsulfenyl fluoride

B

difluoro(trifluoromethyl)trifluormethylsulfanylsulfur(IV)
26391-89-9

difluoro(trifluoromethyl)trifluormethylsulfanylsulfur(IV)

Conditions
ConditionsYield
at 100°C;A 10%
B 90%
at 100°C;A 10%
B 90%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

Hg(2+)*Cl(1-)*OC(CF3)3(1-)=HgCl{OC(CF3)3}

Hg(2+)*Cl(1-)*OC(CF3)3(1-)=HgCl{OC(CF3)3}

Perfluor-tert.-butyl-trifluormethansulfenat
66700-53-6

Perfluor-tert.-butyl-trifluormethansulfenat

Conditions
ConditionsYield
with Hg(Cl)OC(CF3)3 excess at 0°C (24 h);90%
excess of (CF3)3COHgCl, 24 h, 0°C;90%
with Hg(Cl)OC(CF3)3 excess at 0°C (24 h);90%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

acrylic acid methyl ester
292638-85-8

acrylic acid methyl ester

A

CF3SCH2CHClCO2CH3

CF3SCH2CHClCO2CH3

B

α-(Trifluormethylthio)-β-chlorpropionat
34033-72-2

α-(Trifluormethylthio)-β-chlorpropionat

C

2-Chloromethyl-4-trifluoromethylsulfanyl-pentanedioic acid dimethyl ester
34033-73-3

2-Chloromethyl-4-trifluoromethylsulfanyl-pentanedioic acid dimethyl ester

Conditions
ConditionsYield
CF3SCl excess; gas chromy. and (19)F-NMR detection;A 10%
B 90%
C n/a
CF3SCl excess; gas chromy. and (19)F-NMR detection;A 10%
B 90%
C n/a
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

N-Sulfinyl-trifluormethansulfenamid
22089-64-1

N-Sulfinyl-trifluormethansulfenamid

Conditions
ConditionsYield
With N-sulfinyl trimethylsilanamine at 0℃; for 4h; ultrasound;89%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

Se,Se-bis(trifluoromethyl) carbonodiselenothioate
54393-47-4

Se,Se-bis(trifluoromethyl) carbonodiselenothioate

Bis(trifluormethylselenyl)chlormethyl-trifluormethyldisulfan

Bis(trifluormethylselenyl)chlormethyl-trifluormethyldisulfan

Conditions
ConditionsYield
for 2h; Irradiation;88%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

3-oxo-3-phenylpropanamide
3446-58-0

3-oxo-3-phenylpropanamide

A

α,α-bis(trifluoromethylthio)benzoylacetic acid amide

α,α-bis(trifluoromethylthio)benzoylacetic acid amide

B

α-trifluoromethylthio-benzoylacetic acid amide
116073-28-0

α-trifluoromethylthio-benzoylacetic acid amide

Conditions
ConditionsYield
In chloroform Heating; 0 deg C, 30 min, room temperature, 20 h;A 4%
B 88%
Conditions
ConditionsYield
In tetrahydrofuran 20°C for 1.5 h, Carius tube;88%
In tetrahydrofuran 20°C for 1.5 h, Carius tube;88%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

Bis<2,2,4,4-tetrakis(trifluormethyl)-4H-1,3,5-dioxazin-6-ylthio>quecksilber
93383-98-3

Bis<2,2,4,4-tetrakis(trifluormethyl)-4H-1,3,5-dioxazin-6-ylthio>quecksilber

<2,2,4,4-Tetrakis(trifluormethyl)-4H-1,3,5-dioxazin-6-yl>(trifluormethyl)disulfan
103191-46-4

<2,2,4,4-Tetrakis(trifluormethyl)-4H-1,3,5-dioxazin-6-yl>(trifluormethyl)disulfan

Conditions
ConditionsYield
In dichloromethane at -196℃; for 12h;87%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

acetone
67-64-1

acetone

1-trifluoromethylthio-2-propanone
42105-30-6

1-trifluoromethylthio-2-propanone

Conditions
ConditionsYield
bomb tube (-80 to +20°C);86%
bomb tube (-80 to +20°C);86%
71%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

dimedone
126-81-8

dimedone

2-(trifluoromethylthio)-5,5-dimethyl-1,3-cyclohexanedione
128402-12-0

2-(trifluoromethylthio)-5,5-dimethyl-1,3-cyclohexanedione

Conditions
ConditionsYield
With pyridine In chloroform Ambient temperature;86%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

bis(trifluoromethylthio)selenide

bis(trifluoromethylthio)selenide

Conditions
ConditionsYield
With dmap; hydrogen selenide In dichloromethane at -78℃; for 3h;86%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

5-amino-1-(2-chloro-6-fluoro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile
1000815-86-0

5-amino-1-(2-chloro-6-fluoro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile

5-amino-3-cyano-1-(2-chloro-6-fluoro-4-trifluoromethylphenyl)-4-trifluoro-methylthiopyrazole
1000815-85-9

5-amino-3-cyano-1-(2-chloro-6-fluoro-4-trifluoromethylphenyl)-4-trifluoro-methylthiopyrazole

Conditions
ConditionsYield
Stage #1: Trifluoromethylsulfenyl chloride; 5-amino-1-(2-chloro-6-fluoro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile In dichloromethane at 0 - 25℃;
Stage #2: With sodium hydrogencarbonate In dichloromethane; water
86%
2,5-DIMETHYLTHIOPHENE
638-02-8

2,5-DIMETHYLTHIOPHENE

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

2,5-dimethyl-3-trifluoromethylsulfanyl-thiophene
60830-50-4

2,5-dimethyl-3-trifluoromethylsulfanyl-thiophene

Conditions
ConditionsYield
tin(IV) chloride86%
tin(IV) chloride86%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

silver-2,3,4,5-tetrakis(trifluoromethylsulfanyl)-1H-pyrrolide
71940-96-0

silver-2,3,4,5-tetrakis(trifluoromethylsulfanyl)-1H-pyrrolide

1,2,3,4,5-Pentakis(trifluoromethylthio)pyrrole
87840-93-5

1,2,3,4,5-Pentakis(trifluoromethylthio)pyrrole

Conditions
ConditionsYield
at 20℃; for 24h;85%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

N-silver(I) succinimide
55047-82-0

N-silver(I) succinimide

1-((trifluoromethyl)thio)pyrrolidine-2,5-dione

1-((trifluoromethyl)thio)pyrrolidine-2,5-dione

Conditions
ConditionsYield
In diethyl ether 1) -78 deg C to 20 deg C, 16 h, 2) 20 deg C, 24 h;85%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

1,1,1-trifluoro-N-(3-methoxyphenyl)methanesulfonamide
23384-33-0

1,1,1-trifluoro-N-(3-methoxyphenyl)methanesulfonamide

N-(Trifluormethyl-sulfonyl)-4,6-bis-(trifluormethylthio)-3-methoxy-anilin
66476-52-6

N-(Trifluormethyl-sulfonyl)-4,6-bis-(trifluormethylthio)-3-methoxy-anilin

Conditions
ConditionsYield
In pyridine; chloroform -40°C;85%
In pyridine; chloroform -40°C;85%

Trifluoromethanesulphenyl chloride Chemical Properties

Trifluoromethanesulfonyl chloride(421-17-0)'s molecular formula is CClF3S  and its formula weight is 136.52.
Trifluoromethanesulfonyl chloride(421-17-0)'s  chemical synonyms are Methanesulfenyl chloride, trifluoro-;Perfluoromethylsulfenyl chloride;perfluoromethylsulfenylchloride;trifluoro-methanesulfenylchlorid;trifluoromethanesulfenylchloride;trifluoromethane-sulfenylchloride;TRIFLUOROMETHYLSULFENYL CHLORIDE;TRIFLUOROMETHYLSULPHENYL CHLORIDE
The molecular structure of trifluoromethanesulfonyl chloride(421-17-0):

Trifluoromethanesulphenyl chloride Safety Profile

Explosive reaction with chlorine fluorides. When heated to decomposition it emits toxic fumes of F, Cl, and SOx. See also FLUORIDES.
Hazard Codes  T
Risk Statements  26-34
Safety Statements  23-24/25-26-36/37/39-45
RIDADR  3308
Hazard Note  Highly Toxic/Lachrymatory

Trifluoromethanesulphenyl chloride Specification

Descriptors Computed from Structure
IUPAC Name: trifluoromethyl thiohypochlorite(421-17-0)
Canonical SMILES: C(F)(F)(F)SCl
InChI: InChI=1/CClF3S/c2-6-1(3,4)5
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