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Nα-acetyl-6-fluoro-L-tryptophan is a synthetic derivative of the naturally occurring amino acid L-tryptophan. It features a fluorine atom at the 6-position of the indole ring, which imparts unique chemical and biological properties distinct from those of the parent compound. The Nα-acetyl group provides additional protection to the amino group, which can be significant in certain chemical reactions or biological processes. Nα-acetyl-6-fluoro-L-tryptophan is of interest in medicinal chemistry and drug development due to its potential to interact with biological targets in a manner that is altered by the presence of the fluorine atom and the acetyl group. It may be used in the synthesis of more complex molecules or as a probe to study the effects of structural modifications on protein binding and function.

7592-44-1

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7592-44-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7592-44-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7592-44:
(6*7)+(5*5)+(4*9)+(3*2)+(2*4)+(1*4)=121
121 % 10 = 1
So 7592-44-1 is a valid CAS Registry Number.

7592-44-1Downstream Products

7592-44-1Relevant academic research and scientific papers

The facile synthesis of a series of tryptophan derivatives

Blaser, Georg,Sanderson, John M.,Batsanov, Andrei S.,Howard, Judith A.K.

, p. 2795 - 2798 (2008/09/19)

This study reports a facile method for the synthesis of a variety of 5- and 6-substituted tryptophan derivatives that are difficult to prepare using alternative enzymatic approaches. Acylation of an activated amino acid, derived from serine in situ, is coupled with an enzymatic resolution step to furnish enantiopure analogues bearing a range of electron withdrawing and releasing substituents. Isolation of a dehydroalanine derivative as a by-product from some reactions provides some insights into the likely mechanism of the reaction.

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