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128648-60-2

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128648-60-2 Usage

Description

(E)-4-AMINO-4-ETHOXY-1,1,1-TRIFLUOROBUT-3-EN-2-ONE is a chemical compound characterized by the molecular formula C6H8F3NO2. It is a derivative of 1,1,1-trifluoro-4-oxobut-2-ene, featuring a butenone backbone with an amino and ethoxy group attached. (E)-4-AMINO-4-ETHOXY-1,1,1-TRIFLUOROBUT-3-EN-2-ONE is recognized for its unique structure and reactivity, which makes it a valuable building block in the realms of organic synthesis and pharmaceutical research. Its potential applications are diverse, spanning across the development of novel drugs and materials, with specific properties and uses contingent upon the context of its application.

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.

128648-60-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-4-amino-4-ethoxy-1,1,1-trifluorobut-3-en-2-one

1.2 Other means of identification

Product number -
Other names -

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:128648-60-2 SDS

128648-60-2Relevant articles and documents

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

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

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