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N-(TRIFLUOROMETHANESULFONYL)TRIFLUOROACETAMIDE, with the chemical formula C4F9NO4S, is a highly stable and non-reactive chemical compound. It is known for its strong and selective fluorinating properties in organic synthesis, making it a valuable reagent in the synthesis of pharmaceuticals and agrochemicals. The presence of trifluoromethyl and trifluoromethanesulfonyl groups enhances its reactivity towards nucleophiles, allowing for the preparation of various specialty chemicals and diverse fluorinated compounds.

151198-85-5

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151198-85-5 Usage

Uses

Used in Pharmaceutical and Agrochemical Synthesis:
N-(TRIFLUOROMETHANESULFONYL)TRIFLUOROACETAMIDE is used as a strong and selective fluorinating reagent for the synthesis of pharmaceuticals and agrochemicals. Its unique properties and reactivity enable the production of a wide range of fluorinated compounds with potential applications in these industries.
Used in Specialty Chemical Preparation:
N-(TRIFLUOROMETHANESULFONYL)TRIFLUOROACETAMIDE is used as a key intermediate in the preparation of various specialty chemicals. Its high reactivity towards nucleophiles allows for the synthesis of diverse fluorinated compounds, making it a valuable component in the production of specialty chemicals.
Used in Specialty Polymers and Materials Production:
N-(TRIFLUOROMETHANESULFONYL)TRIFLUOROACETAMIDE is used in the production of specialty polymers and materials due to its unique properties and reactivity. Its incorporation into these materials can lead to enhanced performance characteristics and novel applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 151198-85-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,1,9 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 151198-85:
(8*1)+(7*5)+(6*1)+(5*1)+(4*9)+(3*8)+(2*8)+(1*5)=135
135 % 10 = 5
So 151198-85-5 is a valid CAS Registry Number.
InChI:InChI=1/C3HF6NO3S/c4-2(5,6)1(11)10-14(12,13)3(7,8)9/h(H,10,11)

151198-85-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trifluoro-N-(trifluoromethylsulfonyl)acetamide

1.2 Other means of identification

Product number -
Other names N-(Trifluoromethanesulfonyl)trifluoroacetamide

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:151198-85-5 SDS

151198-85-5Downstream Products

151198-85-5Relevant academic research and scientific papers

Trifluoromethylsulfonylimino derivatives of sulfur dioxide and its halogen- and selenium-containing analogs

Yagupol'skii,Kondratenko,Klare,Bezdudnyi,Yagupol'skii

, p. 22 - 25 (2007/10/03)

Reactions of N,N-dichlorotrifluoromethanesulfonamide CF3SO2NCl2 with sulfur, selenium, and CF3SeCl gave compounds containing =NSO2CF3 groups at the sulfur or selenium atom: CF3SO2N=SCl2, CF3SO2N=SeCl2, and CF3SO2N=Se(CF3)Cl, respectively. Heating of CF3SO2N=SCl2 with trifluoroacetic anhydride in the presence of CF3COOH resulted in formation of N-sulfinyl amide CF3SO2N=S=O, and the reaction with CF3SO2NCl2 gave sulfur diimide CF3SO2N=S=NSO2CF3.

Preparation of fluorinated imides

Ye,Noftle

, p. 193 - 196 (2007/10/03)

A direct method for the preparation of trifluoroacetimides has been extended to the preparation of trifluoroacetyl trifluoracetimide and the new compound trifluoromethylsulfuryl trifluoroacetimide. Points concerning previously reported syntheses of trifluoroacetyl isocyanate have also been clarified.

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