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(3-AMINO-1-BENZOFURAN-2-YL)(4-FLUOROPHENYL)METHANONE is a chemical compound that features a benzofuran ring with an attached amino group and a fluorophenyl group connected to a methanone. This unique structure suggests potential applications in medicinal chemistry due to the known biological activity associated with benzofuran and fluorophenyl groups, along with the interactive potential of the amino group with biological targets.
Used in Medicinal Chemistry:
(3-AMINO-1-BENZOFURAN-2-YL)(4-FLUOROPHENYL)METHANONE is used as a compound with potential biological activity for the development of new pharmaceuticals. Its benzofuran and fluorophenyl moieties, along with the amino group, may contribute to its interaction with biological targets, making it a candidate for further research and testing in drug discovery processes.

128170-38-7

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128170-38-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128170-38-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,1,7 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 128170-38:
(8*1)+(7*2)+(6*8)+(5*1)+(4*7)+(3*0)+(2*3)+(1*8)=117
117 % 10 = 7
So 128170-38-7 is a valid CAS Registry Number.

128170-38-7Upstream product

128170-38-7Relevant academic research and scientific papers

Three-step synthesis of an array of substituted benzofurans using polymer-supported reagents

Habermann, Joerg,Ley, Steven V.,Smits, Rene

, p. 2421 - 2423 (2007/10/03)

An efficient combinatorial route to substituted 3-phenyl-benzofurans, is achieved by the bromination of acetophenones to α-bromoacetophenones by polymer-supported pyridinium bromide perbromide (PSPBP). The subsequent clean substitution of the obtained bromides by phenols using 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD-P) and cyclodehydration of the resulting α-phenoxyacetophenones using Amberlyst 15, affords pure products without the need for any chromatographic purification step.

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