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4,4,4-trifluoro-butyric acid benzylamide is a chemical compound with the molecular formula C12H12F3NO2. It is a derivative of butyric acid, featuring a benzylamide group attached to the 4,4,4-trifluorobutyric acid moiety. 4,4,4-trifluoro-butyric acid benzylamide is known for its potential applications in pharmaceuticals and as a chemical intermediate in the synthesis of various organic compounds. Its structure is characterized by the presence of three fluorine atoms attached to the butyric acid backbone, which can significantly influence its reactivity and physical properties. The compound is typically synthesized through a series of chemical reactions and is used in research and development for its unique properties, such as enhanced lipophilicity due to the presence of fluorine atoms.

332-16-1

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332-16-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 332-16-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 332-16:
(5*3)+(4*3)+(3*2)+(2*1)+(1*6)=41
41 % 10 = 1
So 332-16-1 is a valid CAS Registry Number.

332-16-1Downstream Products

332-16-1Relevant academic research and scientific papers

Starting from Styrene: A Unified Protocol for Hydrotrifluoromethylation of Diversified Alkenes

Lin, Jin-Hong,Xiao, Ji-Chang,Yang, Yi-Fei

supporting information, p. 9277 - 9282 (2021/12/06)

In contrast with unactivated alkenes, the corresponding hydrotrifluoromethylation of styrene has remained challenging due to the strong propensity of styrene for oligomerization and polymerization. On the basis of our newly developed trifluoromethylation reagent, TFSP, herein we present a general method for the hydrotrifluoromethylation of styrene under photoredox catalysis. The substrate scope was further extended to unactivated alkenes, acrylates, acrylamides, and vinyl-heteroatom-substituted alkenes. The tunability of this method was showcased via the relevant deprotonative trifluoromethylation and trifluoromethyltrifluoroethoxylation reactions.

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