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N-Fluorobenzenesulfonimide

Product Name
N-Fluorobenzenesulfonimide
CAS No.
133745-75-2
Chemical Name
N-Fluorobenzenesulfonimide
Synonyms
NFSI;N-fluoro-N-(phenylsulfonyl)benzenesulfonamide;NFBS;N-FLUORODIBENZENESULFONIMIDE;N-Fluorobenzenesulfonmide;N-FLUOROBENZENESULFONAMIDE;N-(benzenesulfonyl)-N-fluorobenzenesulfonamide;N-FLUOROBIS(PHENYLSULFONYL)AMINE;N-FLUORODI(BENZENESULFONYL)AMINE;N-Fluorobenzenesulfonimide, N-Fluorodibenzenesulfonimide, NFSI
CBNumber
CB4156620
Molecular Formula
C12H10FNO4S2
Formula Weight
315.34
MOL File
133745-75-2.mol
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N-Fluorobenzenesulfonimide Property

Melting point:
114-116 °C
Boiling point:
471.4±28.0 °C(Predicted)
Density 
1.4466 (estimate)
Flash point:
110℃
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Very soluble in acetonitrile, dichloromethane or THF and less soluble in toluene.
form 
solid
pka
-32.45±0.70(Predicted)
color 
white
BRN 
5348902
InChI
InChI=1S/C12H10FNO4S2/c13-14(19(15,16)11-7-3-1-4-8-11)20(17,18)12-9-5-2-6-10-12/h1-10H
InChIKey
RLKHFSNWQCZBDC-UHFFFAOYSA-N
SMILES
C1(S(N(F)S(C2=CC=CC=C2)(=O)=O)(=O)=O)=CC=CC=C1
CAS DataBase Reference
133745-75-2(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi,O
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
10
Hazard Note 
Oxidising Agent
TSCA 
No
HazardClass 
IRRITANT
HS Code 
29242990
Storage Class
11 - Combustible Solids
Hazard Classifications
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
392715
Product name
N-Fluorobenzenesulfonimide
Purity
97%
Packaging
5g
Price
$90.5
Updated
2025/07/31
Sigma-Aldrich
Product number
392715
Product name
N-Fluorobenzenesulfonimide
Purity
97%
Packaging
500g
Price
$532
Updated
2023/01/07
TCI Chemical
Product number
F0335
Product name
N-Fluorobenzenesulfonimide [Fluorinating Reagent]
Purity
>97.0%(T)
Packaging
5g
Price
$73
Updated
2025/07/31
TCI Chemical
Product number
F0335
Product name
N-Fluorobenzenesulfonimide [Fluorinating Reagent]
Purity
>97.0%(T)
Packaging
25g
Price
$254
Updated
2025/07/31
TRC
Product number
F596833
Product name
N-Fluorobenzenesulfonimide
Packaging
5g
Price
$70
Updated
2021/12/16
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N-Fluorobenzenesulfonimide Chemical Properties,Usage,Production

Chemical Properties

Off-white to light brown crystalline powder

Uses

Versatile fluorinating reagent used in the fluorination of aryls, enolates, carbanions, organolithiums, etc.

Uses

N-Fluorobenzenesulfonimide fluorinates aromatics, enolates, azaenolates and carbanions in high yield. It is used for diastereoselective fluorination of Li enolates of chiral carboximides, for directed fluorination of ortho-lithiated aromatics and for a review of electrophilic N-F fluorinating agents. Asymmteric fluorinations is effected in the presence of a Pd-BINAP catalyst system at room temperature in an ionic liquid. It is a reagent employed in a palladium-catalyzed enantioselective fluorination of t-butoxycarbonyl lactones and lactams. It is also used in the electrophilic difluorination of dihalopyridines with butyl lithium and in the direct conversion of alcohols to dibenzenesulfonamides with triphenylphosphine.

Application

N-Fluorobenzenesulfonimide is a mild electrophilic fluorinating reagent, that can also be used as a strong oxidant for the promotion of reductive elimination from transition metals.

General Description

N-Fluorobenzenesulfonimide (NFSi) is a commonly used electrophilic fluorinating agent in organic synthesis to introduce fluorine into neutral organic molecules. It is also used to fluorinate nucleophilic substrates such as reactive organometallic species and malonate anions.
NFSi can be synthesized by the reaction of benzenesulfonimide with fluorine.

Synthesis

There are two main methods for the production of N-fluorobenzenesulfonamide, the first Differding method, the specific preparation process is: diphenylsulfonimide dissolved in acetonitrile, add sodium fluoride, the mixture cooled down to -35 ?? C, the volume ratio of 1:10 fluorine and nitrogen mixture into the 2h, nitrogen purging for 2h, filtration, evaporation, recrystallization process to obtain the white crystals, the yield is 74%.

The other one is Wanger method, the specific preparation process is as follows: diphenylsulfonamide sodium salt is dissolved in water/acetonitrile or pure water, and after cooling, fluorine and nitrogen mixture with V(F2):V(N2) = 1:10 is passed in, and after the reaction is finished, the reactor is purged with nitrogen, and after filtration, washing and drying, N-fluorosubstituted bisbenzenesulfonamide product is obtained, and the yield can reach 94% at the highest.

N-Fluorobenzenesulfonimide Preparation Products And Raw materials

Raw materials

Preparation Products

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N-Fluorobenzenesulfonimide Suppliers

Changzhou Sunchem Pharmaceutical Chemical Material Co.,Ltd.
Tel
0519-85269522 15906111708
Fax
013660798926
Email
sunlight68@126.com
Country
China
ProdList
100
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60
Shanghai Mixiu Chemical Co., Ltd.
Tel
18101936766
Fax
021-58583907
Email
eileen@shmychem.com
Country
China
ProdList
350
Advantage
55
HuBei ZhuoXi Fluorochemical Co., Ltd.,
Tel
0712-3586991 13801737011
Fax
0712-3586998
Email
xxg@hbzxchem.com
Country
China
ProdList
9
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58
Shanghai Furui Fine Chemicals Co., Ltd.
Tel
021-36041048 13361903612
Fax
86-021-36041048
Email
13361903612@189.cn
Country
China
ProdList
12
Advantage
55
Jiangxi fluopharm chemicals co.,ltd
Tel
021-13916493875 02167659729
Email
rita.liu@fluopharm.com
Country
China
ProdList
22
Advantage
58
Wuhan Xingzhongcheng Technology Co., Ltd.
Tel
027-83389957 18627766980
Fax
027-83389957
Email
914018854@qq.com
Country
China
ProdList
282
Advantage
58
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
INTATRADE GmbH
Tel
+49 3493/605464
Fax
+49 3493/605470
Email
sales@intatrade.de
Country
Germany
ProdList
3572
Advantage
66
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
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View Lastest Price from N-Fluorobenzenesulfonimide manufacturers

Hebei Chuanghai Biotechnology Co., Ltd
Product
N-Fluorobenzenesulfonimide 133745-75-2
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2025-03-10
Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
N-Fluorobenzenesulfonimide 133745-75-2
Price
US $30.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
5000kg/Month
Release date
2024-04-28
Hebei Yanxi Chemical Co., Ltd.
Product
N-Fluorobenzenesulfonimide 133745-75-2
Price
US $0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
10 tons
Release date
2024-01-30

133745-75-2, N-FluorobenzenesulfonimideRelated Search:


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  • CAS:133745-75-2
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  • C12H10NO4FS2
  • C12H10FNO4S2
  • C12H10FN4S2
  • C12H14FNO4S2
  • C6H5SO22NF
  • C12F1H10N1O4S2
  • C-X Bond Formation (Halogen)