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842169-71-5

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842169-71-5 Usage

Description

1-(3-Bromo-phenyl)-2,2,2-trifluoro-ethylamine hydrochloride is a chemical compound that features a trifluoroethylamine group and a 3-bromo-phenyl group, both connected to a central carbon atom. This hydrochloride salt form enhances its stability and water solubility, making it a versatile building block in organic synthesis and pharmaceutical research for creating pharmacologically active compounds.

Uses

Used in Pharmaceutical Research:
1-(3-Bromo-phenyl)-2,2,2-trifluoro-ethylamine hydrochloride is used as a key intermediate in the synthesis of various drugs, leveraging its unique structural features to contribute to the development of new therapeutic agents with potential applications across different medical fields.
Used in Organic Synthesis:
In the realm of organic synthesis, 1-(3-Bromo-phenyl)-2,2,2-trifluoro-ethylamine hydrochloride serves as a valuable precursor for the creation of biologically active molecules, facilitating the design and production of innovative compounds with specific pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 842169-71-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,2,1,6 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 842169-71:
(8*8)+(7*4)+(6*2)+(5*1)+(4*6)+(3*9)+(2*7)+(1*1)=175
175 % 10 = 5
So 842169-71-5 is a valid CAS Registry Number.

842169-71-5Downstream Products

842169-71-5Relevant articles and documents

Synthesis of alpha fluoroalkyl amines

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Page/Page column 8; 9, (2008/06/13)

This invention describes the reaction of an alpha fluoroalkyl ketone with a bis(trialkylsilyl)amide to give a stable N-trialkylsilyl imine. Treatment of the N-trialkylsilyl imine with an alcohol leads to solvolysis of the trialkylsilyl group and yields a

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