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421-83-0 Usage

Uses

Ru(II) complex-catalyzed trifluoromethylating agent for aromatics and alkenes.

Check Digit Verification of cas no

The CAS Registry Mumber 421-83-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,2 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 421-83:
(5*4)+(4*2)+(3*1)+(2*8)+(1*3)=50
50 % 10 = 0
So 421-83-0 is a valid CAS Registry Number.
InChI:InChI=1/CClF3O2S/c2-8(6,7)1(3,4)5

421-83-0 Well-known Company Product Price

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  • (Code)Product description
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  • TCI America

  • (T1027)  Trifluoromethanesulfonyl Chloride  >98.0%(GC)

  • 421-83-0

  • 5g

  • 565.00CNY

  • Detail
  • TCI America

  • (T1027)  Trifluoromethanesulfonyl Chloride  >98.0%(GC)

  • 421-83-0

  • 25g

  • 1,720.00CNY

  • Detail
  • Alfa Aesar

  • (B21774)  Trifluoromethanesulfonyl chloride, 98%   

  • 421-83-0

  • 5g

  • 460.0CNY

  • Detail
  • Alfa Aesar

  • (B21774)  Trifluoromethanesulfonyl chloride, 98%   

  • 421-83-0

  • 25g

  • 1532.0CNY

  • Detail
  • Alfa Aesar

  • (B21774)  Trifluoromethanesulfonyl chloride, 98%   

  • 421-83-0

  • 100g

  • 5819.0CNY

  • Detail
  • Aldrich

  • (164798)  Trifluoromethanesulfonylchloride  ≥99%

  • 421-83-0

  • 164798-5G

  • 446.94CNY

  • Detail
  • Aldrich

  • (164798)  Trifluoromethanesulfonylchloride  ≥99%

  • 421-83-0

  • 164798-25G

  • 1,530.36CNY

  • Detail

421-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name TRIFLUOROMETHANESULFONYL CHLORIDE

1.2 Other means of identification

Product number -
Other names triflic chloride

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:421-83-0 SDS

421-83-0Synthetic route

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%
PCl5*ZnCl2

PCl5*ZnCl2

zinc trifluoromethanesulfonate
54010-75-2

zinc trifluoromethanesulfonate

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
260°C, 2 h;94%
260°C, 2 h;94%
trifluorormethanesulfonic acid
1493-13-6

trifluorormethanesulfonic acid

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
With thionyl chloride; N,N-dimethyl-formamide at 40℃; for 12h; Cooling with ice; Green chemistry;87.5%
With phosphorus pentachloride at 100℃;85%
With phosphorus pentachloride
methanol
67-56-1

methanol

trans-chlorotetrafluoro(trifluoromethyl)sulfur(VI)
25030-42-6, 42179-04-4

trans-chlorotetrafluoro(trifluoromethyl)sulfur(VI)

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
in presence of (CH3)4N, 25°C, 10 h;75%
in presence of (CH3)4N, 25°C, 10 h;75%
chlorine
7782-50-5

chlorine

pentafluoroethanesulfinic acid
344324-36-3

pentafluoroethanesulfinic acid

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
In acetic acid chlorination;74.6%
In acetic acid chlorination;74.6%
benzyl trifluoromethyl sulfide
351-60-0

benzyl trifluoromethyl sulfide

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
With chlorine In water at 5℃; under 3040 Torr; for 2h;70%
(Dichloroiodo)benzene
932-72-9

(Dichloroiodo)benzene

pentafluoroethanesulfinic acid
344324-36-3

pentafluoroethanesulfinic acid

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
chlorination;65.7%
chlorination;65.7%
trifluorormethanesulfonic acid
1493-13-6

trifluorormethanesulfonic acid

phosphorus pentachloride
10026-13-8, 874483-75-7

phosphorus pentachloride

A

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
A 63%
B n/a
A 63%
B n/a
zinc trifluoromethanesulfonate
54010-75-2

zinc trifluoromethanesulfonate

zinc(II) chloride
7646-85-7

zinc(II) chloride

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
anhydr. ZnCl2, heating, Fischer burner, 4 h; fractional distn.;43%
anhydr. ZnCl2, heating, Fischer burner, 4 h; fractional distn.;43%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

dihydrogen peroxide
7722-84-1

dihydrogen peroxide

A

Bis(trifluoromethyl)disulfid
372-64-5

Bis(trifluoromethyl)disulfid

B

trifluorormethanesulfonic acid
1493-13-6

trifluorormethanesulfonic acid

C

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
35% H2O2 soln.;A 35%
B 7%
C 40%
35% H2O2 soln.;A 35%
B 7%
C 40%
trans-chlorotetrafluoro(trifluoromethyl)sulfur(VI)
25030-42-6, 42179-04-4

trans-chlorotetrafluoro(trifluoromethyl)sulfur(VI)

sodium methylate
124-41-4

sodium methylate

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
25°C, 10 h;30%
25°C, 10 h;30%
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
With water; chlorine
trifluoromethylsulfinyl chloride
20621-29-8

trifluoromethylsulfinyl chloride

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
With water
trifluoromethanesulfinyl fluoride
812-12-4

trifluoromethanesulfinyl fluoride

A

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

B

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

C

trifluoromethylsulfinyl chloride
20621-29-8

trifluoromethylsulfinyl chloride

Conditions
ConditionsYield
With hydrogenchloride at -183℃;
zinc trifluoromethanesulfonate
54010-75-2

zinc trifluoromethanesulfonate

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
With PCl5*2ZnCl2 at 260℃;
carbon disulfide
75-15-0

carbon disulfide

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
With sulfur tetrafluoride; hydrogen fluoride; water; chlorine 1.) 80 deg C, 16 h, 2.) 20 deg C, 24 h, 40-50 deg C, 24 h; Yield given. Multistep reaction;
trifluoromethylsulfonic anhydride
358-23-6

trifluoromethylsulfonic anhydride

A

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

B

seleninyl bis(trifluorometanesulfonate)
117950-83-1

seleninyl bis(trifluorometanesulfonate)

Conditions
ConditionsYield
With selenium oxychloride at 60℃;
Langlois reagent
2926-29-6

Langlois reagent

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
With chlorine In water at 0 - 10℃; under 2250.2 Torr; for 2h; Yield given;
trifluoromethanesulfonate
37181-39-8

trifluoromethanesulfonate

A

phosgene
75-44-5

phosgene

B

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
distn.;
trifluoromethylsulfonic anhydride
358-23-6

trifluoromethylsulfonic anhydride

sodium chloride
7647-14-5

sodium chloride

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
In further solvent(s) solvent: tetramethylenesulfone, 3 h;
PCl5*ZnCl2

PCl5*ZnCl2

potassium trifluoromethansulfonate
2926-27-4

potassium trifluoromethansulfonate

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
260°C, 2 h;80-85
260°C, 2 h;80-85
Trifluoromethanesulfonyl fluoride
335-05-7

Trifluoromethanesulfonyl fluoride

chlorine
7782-50-5

chlorine

hydrazine
302-01-2

hydrazine

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
In further solvent(s) redn. of 95% N2H4 in CFCl2CF2Cl at 0-10°C, after addn. of Cl2;
trifluoromethylsulfinyl chloride
20621-29-8

trifluoromethylsulfinyl chloride

water
7732-18-5

water

A

Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

B

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

trifluoromethyl hypochlorite
22082-78-6

trifluoromethyl hypochlorite

trifluoromethylsulfinyl chloride
20621-29-8

trifluoromethylsulfinyl chloride

A

thionyl chlorofluoride
14177-25-4

thionyl chlorofluoride

B

carbon tetrafluoride
75-73-0

carbon tetrafluoride

C

Carbonyl fluoride
353-50-4

Carbonyl fluoride

D

chlorotrifluoromethane
75-72-9

chlorotrifluoromethane

E

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
25°C, 2 h; further products;
25°C, 2 h; further products;
trans-chlorotetrafluoro(trifluoromethyl)sulfur(VI)
25030-42-6, 42179-04-4

trans-chlorotetrafluoro(trifluoromethyl)sulfur(VI)

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
With NaOCH3 25°C, 10 h;
With CH3OH in presence of (CH3)3N, 25°C, 10 h;
ortho-chlorobenzyl trifluoromethylsulfide

ortho-chlorobenzyl trifluoromethylsulfide

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
With water; chlorine at 10 - 30℃; under 73.5572 - 735.572 Torr;
trifluoromethan
75-46-7

trifluoromethan

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Conditions
ConditionsYield
With rhodium(III) chloride; sulfuryl dichloride; sulfuric acid; dihydrogen peroxide; urea at 65℃; for 12h;
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

chlorotrifluoromethane
75-72-9

chlorotrifluoromethane

Conditions
ConditionsYield
With copper at 200℃; for 24h;100%
With pyridine; copper dichloride In 1,4-dioxane at 100℃; for 1h; Inert atmosphere; Schlenk technique;8 %Spectr.
3',5'-bis-O-(tert-butyldimethylsilyl)-β-D-adenosine
69504-03-6

3',5'-bis-O-(tert-butyldimethylsilyl)-β-D-adenosine

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

9-[3,5-bis-O-[(1,1-dimethylethyl)dimethylsilyl]-2-trifluoromethylsulfonyloxy-β-D-arabinofuranosyl]-9H-purin-6-amine
118525-28-3

9-[3,5-bis-O-[(1,1-dimethylethyl)dimethylsilyl]-2-trifluoromethylsulfonyloxy-β-D-arabinofuranosyl]-9H-purin-6-amine

Conditions
ConditionsYield
With dmap; triethylamine In pyridine at 0 - 20℃; for 3h; Esterification;100%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

9-[3-O-benzoyl-5-O-(triphenylmethyl)-β-D-ribofuranosyl]-6-chloro-9H-purine
234436-48-7

9-[3-O-benzoyl-5-O-(triphenylmethyl)-β-D-ribofuranosyl]-6-chloro-9H-purine

5'-O-trityl-3'-O-benzoyl-2'-O-trifluoromethanesulfonyl-6-chloropurine riboside
339196-22-4

5'-O-trityl-3'-O-benzoyl-2'-O-trifluoromethanesulfonyl-6-chloropurine riboside

Conditions
ConditionsYield
With dmap In toluene100%
With dmap In toluene
(2-hydroxy-6-methoxy-naphthalen-1-yl)-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-methanone
649724-98-1

(2-hydroxy-6-methoxy-naphthalen-1-yl)-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-methanone

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

trifluoro-methanesulfonic acid 6-methoxy-1-[4-(2-piperidin-1-yl-ethoxy)-benzoyl]-naphthalen-2-yl ester
648905-79-7

trifluoro-methanesulfonic acid 6-methoxy-1-[4-(2-piperidin-1-yl-ethoxy)-benzoyl]-naphthalen-2-yl ester

Conditions
ConditionsYield
With pyridine In dichloromethane at 0℃; for 0.25h;100%
With pyridine In dichloromethane at 0℃; for 0.25h;100%
Stage #1: (2-hydroxy-6-methoxy-naphthalen-1-yl)-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-methanone; trifluoromethane sulfonyl chloride With pyridine In dichloromethane for 0.5h;
Stage #2: With water In dichloromethane
100%
7-hydroxy-8-nitro-1,2,4,5-tetrahydrobenzo[d]azepine-3-carboxylic acid tert-butyl ester
583047-16-9

7-hydroxy-8-nitro-1,2,4,5-tetrahydrobenzo[d]azepine-3-carboxylic acid tert-butyl ester

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

7-nitro-8-trifluoromethanesulfonyloxy-1,2,4,5-tetrahydrobenzo[d]azepine-3-carboxylic acid tert-butyl ester
583047-17-0

7-nitro-8-trifluoromethanesulfonyloxy-1,2,4,5-tetrahydrobenzo[d]azepine-3-carboxylic acid tert-butyl ester

Conditions
ConditionsYield
With triethylamine In acetone at 20℃; for 1h;100%
With triethylamine In acetone at 0℃; for 0.5h;87%
In acetone at 0 - 20℃; for 2h; Product distribution / selectivity;
[trans-4-(4-hydroxyphenyl)cyclohexyl]acetic acid methyl ester

[trans-4-(4-hydroxyphenyl)cyclohexyl]acetic acid methyl ester

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

methyl [trans-4-(4-{[(trifluoromethyl)sulfonyl]oxy}phenyl)cyclohexyl]acetate

methyl [trans-4-(4-{[(trifluoromethyl)sulfonyl]oxy}phenyl)cyclohexyl]acetate

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 4 - 15℃; for 17.25h;100%
With N-ethyl-N,N-diisopropylamine In dichloromethane at 4 - 15℃; for 17.25h;100%
trans-[4-(4-hydroxyphenyl)cyclohexyl]acetic methyl ester
701232-67-9

trans-[4-(4-hydroxyphenyl)cyclohexyl]acetic methyl ester

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

(trans)-methyl 2-(4-(4-(((trifluoromethyl)sulfonyl)oxy)phenyl)cyclohexyl)acetate
701232-68-0

(trans)-methyl 2-(4-(4-(((trifluoromethyl)sulfonyl)oxy)phenyl)cyclohexyl)acetate

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 4 - 15℃; for 17.25h;100%
With N-ethyl-N,N-diisopropylamine In dichloromethane at 4 - 15℃; for 17.25h;100%
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0 - 20℃;
9-(3,5-O-isopropylidene-β-L-xylofuranosyl)adenine
339091-27-9

9-(3,5-O-isopropylidene-β-L-xylofuranosyl)adenine

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

9-(3,5-O-isopropylidene-2-O-triflyl-β-L-xylofuranosyl)adenine
339091-34-8

9-(3,5-O-isopropylidene-2-O-triflyl-β-L-xylofuranosyl)adenine

Conditions
ConditionsYield
With pyridine at 20℃;100%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

trifluoro-methanesulfonic acid 6-methoxy-1-[4-(2-piperidin-1-yl-ethoxy)-benzoyl]-naphthalen-2-yl ester
648905-79-7

trifluoro-methanesulfonic acid 6-methoxy-1-[4-(2-piperidin-1-yl-ethoxy)-benzoyl]-naphthalen-2-yl ester

Conditions
ConditionsYield
Stage #1: (2-hydroxy-6-methoxy-naphthalen-1-yl)-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-methanone With pyridine In dichloromethane at 0℃;
Stage #2: trifluoromethane sulfonyl chloride In dichloromethane for 0.5h;
Stage #3: With water In dichloromethane
100%
9-[2'-O-tert-butyldimethylsilyl-5'-O-(4,4'-dimethoxytrityl)-xylofuranosyl]adenine
1005482-75-6

9-[2'-O-tert-butyldimethylsilyl-5'-O-(4,4'-dimethoxytrityl)-xylofuranosyl]adenine

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

9-[2'-O-tert-butyldimethylsilyl-5'-O-(4,4'-dimethoxytrityl)-3'-O-trifluoromethanesulfonyl-xylofuranosyl]adenine
1005482-78-9

9-[2'-O-tert-butyldimethylsilyl-5'-O-(4,4'-dimethoxytrityl)-3'-O-trifluoromethanesulfonyl-xylofuranosyl]adenine

Conditions
ConditionsYield
With dmap In dichloromethane at 0℃; for 1h;100%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

triethylamine
121-44-8

triethylamine

acetylacetone
123-54-6

acetylacetone

3,3-dichloropentane-2,4-dione
33657-50-0

3,3-dichloropentane-2,4-dione

Conditions
ConditionsYield
In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

triethylamine
121-44-8

triethylamine

malonic acid dimethyl ester
108-59-8

malonic acid dimethyl ester

dimethyl 2,2-dichloromalonate
29653-30-3

dimethyl 2,2-dichloromalonate

Conditions
ConditionsYield
In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

ethyl acetoacetate
141-97-9

ethyl acetoacetate

triethylamine
121-44-8

triethylamine

ethyl 2,2-dichloroacetoacetate
6134-66-3

ethyl 2,2-dichloroacetoacetate

Conditions
ConditionsYield
In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

triethylamine
121-44-8

triethylamine

methyl 2-cyanoacetate
105-34-0

methyl 2-cyanoacetate

methyl dichlorocyanoacetate
25761-68-6

methyl dichlorocyanoacetate

Conditions
ConditionsYield
In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

acetylacetone
123-54-6

acetylacetone

3,3-dichloropentane-2,4-dione
33657-50-0

3,3-dichloropentane-2,4-dione

Conditions
ConditionsYield
With 1,5-Diazabicyclo[5.4.0]undec-5-ene In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
With 1,5-diazabicyclo(5.4.0)undec-5-ene In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

phosphonic acid diethyl ester
762-04-9

phosphonic acid diethyl ester

diethyl chlorophosphate
814-49-3

diethyl chlorophosphate

Conditions
ConditionsYield
With 1,5-Diazabicyclo[5.4.0]undec-5-ene In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
With 1,5-diazabicyclo(5.4.0)undec-5-ene In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

malonic acid dimethyl ester
108-59-8

malonic acid dimethyl ester

dimethyl 2,2-dichloromalonate
29653-30-3

dimethyl 2,2-dichloromalonate

Conditions
ConditionsYield
With 1,5-Diazabicyclo[5.4.0]undec-5-ene In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
With 1,5-diazabicyclo(5.4.0)undec-5-ene In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

ethyl acetoacetate
141-97-9

ethyl acetoacetate

ethyl 2,2-dichloroacetoacetate
6134-66-3

ethyl 2,2-dichloroacetoacetate

Conditions
ConditionsYield
With 1,5-Diazabicyclo[5.4.0]undec-5-ene In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
With 1,5-diazabicyclo(5.4.0)undec-5-ene In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

methyl 2-cyanoacetate
105-34-0

methyl 2-cyanoacetate

methyl dichlorocyanoacetate
25761-68-6

methyl dichlorocyanoacetate

Conditions
ConditionsYield
With 1,5-Diazabicyclo[5.4.0]undec-5-ene In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
With 1,5-diazabicyclo(5.4.0)undec-5-ene In dichloromethane 1:1 molar mixture of educts per acidic hydrogen, 20-25°C, 1 h;100%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

diethyl malonate
105-53-3

diethyl malonate

A

diethyl dichloromalonate
20165-81-5

diethyl dichloromalonate

B

trifluoromethanesulfinic acid
34642-42-7

trifluoromethanesulfinic acid

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 10 - 50℃; Mechanism; Reagent/catalyst; Solvent;A 100%
B n/a
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

1,2-diamino-benzene
95-54-5

1,2-diamino-benzene

p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

4-methyl-N-{[2-(trifluoromethyl)sulfonamide]phenyl}benzenesulfonamide

4-methyl-N-{[2-(trifluoromethyl)sulfonamide]phenyl}benzenesulfonamide

Conditions
ConditionsYield
With trifluoromethylsulfonic anhydride In dichloromethane at -78℃;100%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

Estrone
53-16-7

Estrone

estrone triflate
92817-04-4

estrone triflate

Conditions
ConditionsYield
With pyridine In dichloromethane at 20℃; for 0.25h; Inert atmosphere;99%
With triethylamine91%
With dmap; triethylamine In dichloromethane at 0 - 20℃; for 6h; Inert atmosphere;82%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

hydroxy(phenyl)-λ3-iodanyl diphenylphosphinate
189581-08-6

hydroxy(phenyl)-λ3-iodanyl diphenylphosphinate

C19H15F3IO5PS

C19H15F3IO5PS

Conditions
ConditionsYield
In dichloromethane at 20℃; for 0.25h;99%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

N-tosyl-(4-pentenyl)amine
81097-24-7

N-tosyl-(4-pentenyl)amine

N-(4-chloro-6,6,6-trifluorohexyl)-4-methylbenzenesulfonamide
1569453-40-2

N-(4-chloro-6,6,6-trifluorohexyl)-4-methylbenzenesulfonamide

Conditions
ConditionsYield
With dipotassium hydrogenphosphate; tris(1,10-phenanthroline)ruthenium(II) dichloride In acetonitrile at 25℃; for 15h; Reagent/catalyst; Solvent; Inert atmosphere; Irradiation; regioselective reaction;99%
With dipotassium hydrogenphosphate; tris(1,10-phenanthroline)ruthenium(II) dichloride In acetonitrile at 25℃; for 15h; Catalytic behavior; Reagent/catalyst; Solvent; Photolysis; Inert atmosphere; regioselective reaction;32 mg
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

N-(but-3-en-1-yl)-4-chlorobenzamide
1569453-21-9

N-(but-3-en-1-yl)-4-chlorobenzamide

4-chloro-N-(3-chloro-5,5,5-trifluoropentyl)benzamide
1569453-73-1

4-chloro-N-(3-chloro-5,5,5-trifluoropentyl)benzamide

Conditions
ConditionsYield
With dipotassium hydrogenphosphate; tris(1,10-phenanthroline)ruthenium(II) dichloride In acetonitrile at 25℃; for 15h; Inert atmosphere; Irradiation; Sealed tube; regioselective reaction;99%
6-chloroindole
17422-33-2

6-chloroindole

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

6-chloro-3-((trifluoromethyl)thio)-1H-indole

6-chloro-3-((trifluoromethyl)thio)-1H-indole

Conditions
ConditionsYield
With 1,2,2,3,4,4-hexamethylphosphetane 1-oxide; phenylsilane In 1,4-dioxane at 40℃; Schlenk technique; Sealed tube; Inert atmosphere;99%
With triphenylphosphine; sodium iodide In acetonitrile at 60℃; for 4h; Schlenk technique; Inert atmosphere;91%
With phosphonic acid diethyl ester In acetonitrile at 90℃; for 10h;80%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

5-methoxycarbonylindole
1011-65-0

5-methoxycarbonylindole

3-trifluoromethylsulfanyl-5,1H-indolecarboxylc acid methyl ester
1045823-02-6

3-trifluoromethylsulfanyl-5,1H-indolecarboxylc acid methyl ester

Conditions
ConditionsYield
With 1,2,2,3,4,4-hexamethylphosphetane 1-oxide; phenylsilane In 1,4-dioxane at 40℃; Schlenk technique; Sealed tube; Inert atmosphere;99%
With triphenylphosphine; sodium iodide In acetonitrile at 60℃; for 22h; Schlenk technique; Inert atmosphere;90%
1-tetradecene
1120-36-1

1-tetradecene

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

3-chloro-1,1,1-trifluoropentadecane

3-chloro-1,1,1-trifluoropentadecane

Conditions
ConditionsYield
With [5,10,15,20-tetraphenylporphyrin]cobalt(III) chloride; Langlois reagent In acetonitrile at 100℃; for 12h; Inert atmosphere; Sealed tube;99%
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

trifluoromethylsulfonimide lithium salt

trifluoromethylsulfonimide lithium salt

bis(trifluoromethane)sulfonimide lithium
90076-65-6

bis(trifluoromethane)sulfonimide lithium

Conditions
ConditionsYield
With lithium carbonate In acetonitrile Reagent/catalyst;98.8%

421-83-0Relevant articles and documents

Kitazume,T.,Shreeve,J.M.

, p. 3690 - 3695 (1977)

Transition-Metal-Free Electrophilic Fluoroalkanesulfinylation of Electron-Rich (Het)Arenes with Fluoroalkyl Heteroaryl Sulfones via C(Het)?S and S=O Bond Cleavage

Wei, Jun,Bao, Kun,Qi, Chengcheng,Liu, Yao,Ni, Chuanfa,Sheng, Rong,Hu, Jinbo

supporting information, p. 5528 - 5533 (2019/11/14)

A novel Ph2P(O)Cl-mediated direct fluoroalkanesulfinylation of electron-rich (het)arenes using fluoroalkyl heteroaryl sulfones as the RfSO source (Rf=C4F9, CF2Cl, CF2Br, and CF2COOEt) was developed. This is the first example where 2-HetSO2Rf performs as the RfSO synthon in organic synthesis via both C(Het)?S and S=O bond cleavage. (Figure presented.).

Synthesis method of trimethoxystilbene

-

Paragraph 0014, (2016/10/09)

The invention discloses a synthesis method of trimethoxystilbene. The method comprises the following steps of (1) at room temperature, adding trifluoromethanesulfonic acid into dichloromethane; stirring the mixture; slowly dripping sulfoxide chloride; after the dripping is completed, performing stirring reaction for 12 hours at room temperature; concentrating a reaction system to obtain a coarse product of trifluoromethanesulfonyl chloride; (2) adding aniline and triethylamine into dichloromethane; lowering the temperature to 0 DEG C; dripping the obtained coarse product of trifluoromethanesulfonyl chloride through a dropping funnel; after the dripping is completed, raising the temperature to room temperature for reaction for 2 hours; performing water washing, drying and concentration on the reaction system; then, performing recrystallization by petroleum ether to obtain trimethoxystilbene. The synthesis method has the beneficial effects that the raw materials of trifluoromethanesulfonic acid used by the synthesis method of trimethoxystilbene provided by the invention are common chemical raw materials; the price is low; the acquisition is easy; the cost is greatly reduced; special equipment such as low-temperature kettles is not needed in the production process; the operation is easy; the method is suitable for industrial production.

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