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2,2,2-Trifluoro-1-(4-fluoro-phenyl)-ethylamine is a chemical compound characterized by the molecular formula C8H8F4N. It is a fluorinated amine with a trifluoromethyl group and a fluorophenyl group attached to the amine nitrogen. This unique structure and its fluorinated nature endow it with potential applications across various fields, including pharmaceuticals, agrochemicals, and materials science. It serves as a building block in the synthesis of various fluorine-containing compounds and may exhibit biological activity or other functional properties. However, due to its potential hazardous nature, safety data should be consulted before handling 2,2,2-TRIFLUORO-1-(4-FLUORO-PHENYL)-ETHYLAMINE.

852443-99-3

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852443-99-3 Usage

Uses

Used in Pharmaceutical Industry:
2,2,2-Trifluoro-1-(4-fluoro-phenyl)-ethylamine is used as a building block for the synthesis of pharmaceutical compounds, leveraging its unique structure and fluorinated nature to enhance the properties of the resulting drugs. The incorporation of fluorine atoms can improve the pharmacokinetics, bioavailability, and potency of the final drug products.
Used in Agrochemical Industry:
In the agrochemical sector, 2,2,2-Trifluoro-1-(4-fluoro-phenyl)-ethylamine is utilized as a precursor in the development of new agrochemicals, such as pesticides and herbicides. Its fluorinated structure can contribute to the increased effectiveness and selectivity of these compounds, leading to improved crop protection.
Used in Materials Science:
2,2,2-Trifluoro-1-(4-fluoro-phenyl)-ethylamine is employed in materials science for the synthesis of novel materials with specific properties. Its fluorinated nature can impart unique characteristics to the resulting materials, such as enhanced thermal stability, chemical resistance, or specific electronic properties, making them suitable for various applications in industries like electronics, automotive, and aerospace.

Check Digit Verification of cas no

The CAS Registry Mumber 852443-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,4,4 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 852443-99:
(8*8)+(7*5)+(6*2)+(5*4)+(4*4)+(3*3)+(2*9)+(1*9)=183
183 % 10 = 3
So 852443-99-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H7F4N/c9-6-3-1-5(2-4-6)7(13)8(10,11)12/h1-4,7H,13H2

852443-99-3 Well-known Company Product Price

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  • Aldrich

  • (JWP00325)  2,2,2-Trifluoro-1-(4-fluoro-phenyl)-ethylamine  AldrichCPR

  • 852443-99-3

  • JWP00325-1G

  • 7,733.70CNY

  • Detail

852443-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trifluoro-1-(4-fluorophenyl)ethanamine

1.2 Other means of identification

Product number -
Other names [2,2,2-trifluoro-1-(4-fluorophenyl)ethyl]amine

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:852443-99-3 SDS

852443-99-3Downstream Products

852443-99-3Relevant academic research and scientific papers

Silver-catalyzed formal [3+2]-cycloaddition of α-trifluoromethylated methyl isocyanides: a facile stereoselective synthesis of CF3-substituted heterocycles

Zhang, Xue,Wang, Xin,Gao, Yuelei,Xu, Xianxiu

supporting information, p. 2427 - 2430 (2017/03/01)

An Ag-catalyzed formal [3+2]-cycloaddition of α-trifluoromethylated methyl isocyanides with polar double bonds has been developed for the facile access to trifluoromethylated oxazolines, imidazolines and pyrrolines under mild conditions. The practicality of this chemistry is demonstrated by the gram-scale synthesis of oxazolines with excellent yields and facile transformations of the formed oxazolines to trifluoromethylated β-amino alcohols in quantitative yields.

PYRAZOLE DERIVATIVES AS INHIBITORS OF RECEPTOR TYROSYNE KINASES

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Page/Page column 92, (2008/06/13)

Compounds of formula (I): and their use in the inhibition of Trk activity are described.

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