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2,2,2-trifluoro-N-[2-[(2,2,2-trifluoroacetyl)amino]ethyl]acetamide is a synthetic compound with the chemical formula C6H6F6N2O2. It is a derivative of acetamide and contains trifluoro groups, which are known for their high electronegativity. 2,2,2-trifluoro-N-[2-[(2,2,2-trifluoroacetyl)amino]ethyl]acetamide is often used as a reagent in organic synthesis for the introduction of trifluoromethyl groups into various molecules. Due to its unique structure and properties, it has potential applications in pharmaceutical and agrochemical industries for the development of new materials and drug molecules with enhanced properties. Additionally, it is an important intermediate in the production of various organic compounds and can serve as a building block for the synthesis of more complex chemical structures.

360-43-0

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360-43-0 Usage

Uses

Used in Pharmaceutical Industry:
2,2,2-trifluoro-N-[2-[(2,2,2-trifluoroacetyl)amino]ethyl]acetamide is used as a reagent for the introduction of trifluoromethyl groups into drug molecules, which can enhance their properties and improve their therapeutic effects.
Used in Agrochemical Industry:
2,2,2-trifluoro-N-[2-[(2,2,2-trifluoroacetyl)amino]ethyl]acetamide is used as a reagent for the introduction of trifluoromethyl groups into agrochemical molecules, which can improve their efficacy and selectivity.
Used in Organic Synthesis:
2,2,2-trifluoro-N-[2-[(2,2,2-trifluoroacetyl)amino]ethyl]acetamide is used as an intermediate for the production of various organic compounds, serving as a building block for the synthesis of more complex chemical structures.

Check Digit Verification of cas no

The CAS Registry Mumber 360-43-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 360-43:
(5*3)+(4*6)+(3*0)+(2*4)+(1*3)=50
50 % 10 = 0
So 360-43-0 is a valid CAS Registry Number.

360-43-0Downstream Products

360-43-0Relevant academic research and scientific papers

Ethyl trifluoroacetate: A powerful reagent for differentiating amino groups

Xu, Daqiang,Prasad, Kapa,Repic, Oljan,Blacklock, Thomas J.

, p. 7357 - 7360 (1995)

Selective protection of primary amines in the presence of secondary amines and monofunctionalization of symmetric primary and secondary diamines using ethyl trifluoroacetate is described. Effective differentiation of primary, secondary and tertiary alkyl-substituted primary amines from one another by ethyl trifluoroacetate acylation is also demonstrated. These results are explained on the basis of steric and electronic effects of the substrate amines.

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