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4-Isoxazolecarboxylic acid, 3-ethyl-5-(trifluoroMethyl)-, ethyl, also known as EFMT, is a chemical compound characterized by its molecular formula C9H9F3N2O3. It is a white to off-white crystalline powder that exhibits solubility in organic solvents but is insoluble in water. EFMT serves as a versatile building block in the synthesis of pharmaceuticals and agrochemicals, making it a valuable component in the development of various chemical products.

363617-95-2

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363617-95-2 Usage

Uses

Used in Pharmaceutical Industry:
EFMT is utilized as an intermediate in the production of pharmaceutical compounds, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
EFMT is employed as a herbicide, fungicide, and insecticide, playing a crucial role in controlling pests and diseases in agriculture to ensure crop protection and yield enhancement.
Used in Chemical Synthesis:
As a building block, EFMT is used in the synthesis of a wide range of chemical products, including pharmaceuticals and agrochemicals, due to its unique chemical properties and reactivity.
Safety Considerations:
EFMT is considered a potentially hazardous chemical and should be handled with care, adhering to proper safety protocols and procedures to minimize risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 363617-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,3,6,1 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 363617-95:
(8*3)+(7*6)+(6*3)+(5*6)+(4*1)+(3*7)+(2*9)+(1*5)=162
162 % 10 = 2
So 363617-95-2 is a valid CAS Registry Number.

363617-95-2Upstream product

363617-95-2Downstream Products

363617-95-2Relevant academic research and scientific papers

Convenient synthesis of 5-perfluoroalkylsubstituted isoxazoles

Weimin, Peng,Shizheng, Zhu,Guifang, Jin

, p. 5781 - 5784 (2001)

5-Perfluoroalkylsubstituted isoxazoles are prepared readily from the reaction of nitrile oxide generated in situ from RCH2NO2, TEA and POCl3 with ethyl 3-perfluoroalkyl-3-pyrrolidino-acrylates, which were obtained by treat

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