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L-Phenylalanine, 3-fluoro, hydrochloride is a chemical compound with the molecular formula C9H10ClFNO2. It is a derivative of the naturally occurring amino acid L-phenylalanine, featuring a fluorine atom at the 3-position of the phenyl ring. This modification can significantly alter the properties and reactivity of the molecule compared to the parent compound. The hydrochloride salt form of 3-fluoro-L-phenylalanine is commonly used to improve the solubility and stability of the compound, making it more suitable for various applications in research and pharmaceutical development. L-Phenylalanine, 3-fluoro-, hydrochloride is often employed in the synthesis of pharmaceuticals, as a building block for the development of new drugs, and in studies investigating the effects of structural modifications on protein function and activity.

7655-65-4

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7655-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7655-65-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,5 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7655-65:
(6*7)+(5*6)+(4*5)+(3*5)+(2*6)+(1*5)=124
124 % 10 = 4
So 7655-65-4 is a valid CAS Registry Number.

7655-65-4Downstream Products

7655-65-4Relevant academic research and scientific papers

Chirality-Driven Mode of Binding of α-Aminophosphonic Acid-Based Allosteric Inhibitors of the Human Farnesyl Pyrophosphate Synthase (hFPPS)

Feng, Yuting,Park, Jaeok,Li, Shi-Guang,Boutin, Rebecca,Viereck, Peter,Schilling, Matthew A.,Berghuis, Albert M.,Tsantrizos, Youla S.

, p. 9691 - 9702 (2019/11/03)

Thienopyrimidine-based allosteric inhibitors of the human farnesyl pyrophosphate synthase (hFPPS), characterized by a chiral α-aminophosphonic acid moiety, were synthesized as enantiomerically enriched pairs, and their binding mode was investigated by X-ray crystallography. A general consensus in the binding orientation of all (R)- and (S)-enantiomers was revealed. This finding is a prerequisite for establishing a reliable structure-activity relationship (SAR) model.

UNUSUAL AMINO ACIDS II. Asymmetric Synthesis of Fluorine Containing Phenylalanines

Krause, Hans-Walter,Kreuzfeld, Hans-Joern,Doebler, Christian,Taudien, Stefan

, p. 555 - 566 (2007/10/02)

Few (Z)-α-N-benzoylamino-β-(fluorophenyl)-acrylic acids and their esters were prepared by known procedures and hydrogenated to the corresponding optically active α-benzoyl-β-(fluorophenyl)-alanine derivatives with optical yields up to 90percent using the

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