128648-60-2 Usage
Uses
Used in Pharmaceutical Research:
(E)-4-AMINO-4-ETHOXY-1,1,1-TRIFLUOROBUT-3-EN-2-ONE is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the creation of new drugs with potentially improved therapeutic properties, such as enhanced efficacy, selectivity, and reduced side effects.
Used in Organic Synthesis:
In the field of organic synthesis, (E)-4-AMINO-4-ETHOXY-1,1,1-TRIFLUOROBUT-3-EN-2-ONE serves as a versatile building block for the development of a wide range of chemical products. Its reactivity and structural features enable the synthesis of complex molecules with specific functionalities, which can be applied in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Material Science:
(E)-4-AMINO-4-ETHOXY-1,1,1-TRIFLUOROBUT-3-EN-2-ONE is utilized as a component in the development of advanced materials. Its incorporation into material formulations can lead to enhanced properties such as improved mechanical strength, thermal stability, or chemical resistance, depending on the specific application and industry requirements.
Used in Chemical Research:
As a compound with unique structural and reactive features, (E)-4-AMINO-4-ETHOXY-1,1,1-TRIFLUOROBUT-3-EN-2-ONE is employed in chemical research to explore new reaction pathways, mechanisms, and the synthesis of novel compounds. This contributes to the advancement of chemical knowledge and the discovery of new applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 128648-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,6,4 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 128648-60:
(8*1)+(7*2)+(6*8)+(5*6)+(4*4)+(3*8)+(2*6)+(1*0)=152
152 % 10 = 2
So 128648-60-2 is a valid CAS Registry Number.
128648-60-2Relevant academic research and scientific papers
PYRAZOLE-SUBSTITUTED PYRROLIDINONES AS HERBICIDES
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Page/Page column 29, (2020/12/11)
Disclosed are compounds of Formula (1), including all stereoisomers, N-oxides, and salts thereof, wherein Q is selected from the group consisting of and R1, R2, R3, Y, R4, R5, n, R6, W and
SULFONYLUREAS AND RELATED COMPOUNDS AND USE OF SAME
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Page/Page column 140, (2016/09/15)
ABSTRACT The present invention provides for certain sulfonyl ureas and related compounds which have advantageous properties and show useful activity in the inhibition of activation of the NLRP3 inflammasome. Such compounds are useful in the treatment of a wide range of disorders in which the inflammation process, or more specifically the NLRP3 inflammasome, have been implicated as being a key factor.
Synthesis of novel 3-amino-5-trifluoromethylazoles: A convenient method of obtaining N-(azol-3-yl)amines
Martins, Marcos A. P.,Cunico, Wilson,Brondani, Sergio,Peres, Rodrigo L.,Zimmermann, Nilo,Rosa, Fernanda A.,Fiss, Gabriela F.,Zanatta, Nilo,Bonacorso, Helio G.
, p. 1485 - 1493 (2007/10/03)
A convenient method to obtain 10 3-amino-5-trifluoromethyl-5-hydroxy-4,5- dihydroisoxazoles and 18 3-amino-5-trifluoromethyl-1H-pyrazoles by cyclocondensation reaction of 4-amino-4-ethoxy-1,1,1,-trifluorobut-3-en-2-ones [CF3COCH=C(OEt)NHR, wher
Facile Synthesis of β-Trifluoroacetylketene O,N-, S,N- and N,N-Acetals
Hojo, Masaru,Masuda, Ryoichi,Okada, Etsuji,Yamamoto, Hiromi,Morimoto, Katsushi,Okada, Ken
, p. 195 - 198 (2007/10/02)
Trifluoroacetylketene O,N-, S,N- and N,N-acetals 3-6 are easily obtained in excellent yields by O-N and S-N exchange reactions of trifluoroacetylketene O,O- and S,S-acetals 1, 2 with various amines.
