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47296

o-Fluor-L-phenylalanin

Name: <I>o</I>-Fluor-<SC>L</SC>-phenylalanin
Brand: ALDRICH

puriss., ≥99.0% (sum of enantiomers, HPLC)

Synonym(e):

2-Fluor-L-phenylalanin

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About This Item

Empirische Formel (Hill-System):

C₉H₁₀FNO₂

CAS-Nummer:

19883-78-4

Molekulargewicht:

183.18

Beilstein:

2805791

MDL-Nummer:

MFCD00066448

UNSPSC-Code:

12352200

PubChem Substanz-ID:

24870852

Qualität

puriss.

Assay

≥99.0% (sum of enantiomers, HPLC)

Optische Aktivität

[α]20/D −14±1°, c = 1% in H₂O

Optische Reinheit

enantiomeric ratio: ≥99.5:0.5 (TLC)

SMILES String

N[C@@H](Cc1ccccc1F)C(O)=O

Verpackung

Bottomless glass bottle. Contents are inside inserted fused cone.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number

264687/1

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Accumulation of L-[2-(F-18)]fluorophenylalanine in peri-infarct area in a patient with acute cerebral infarction.

J Hatazawa et al.

Annals of nuclear medicine, 8(3), 213-217 (1994-08-01)

We studied the brain uptake of amino acid in a patient with acute cerebral infarction with L-[2-(F-18)]fluorophenylalanine and positron emission tomography. The increased accumulation of the ligand was specifically found in the peri-infarct area where oxygen metabolism was still maintained

Aging effect on neutral amino acid transport at the blood-brain barrier measured with L-[2-18F]-fluorophenylalanine and PET.

H Ito et al.

Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 36(7), 1232-1237 (1995-07-01)

Neutral amino acids (NAAs) are transported from the blood to the brain using the same carrier system in a competitive fashion. The purpose of this study is to establish a method for evaluating neutral amino acid transport at the blood-brain

Enantioseparation of amino acids, alpha-hydroxy acids, and dipeptides by ligand-exchange CEC using silica-based chiral stationary phases.

Elfriede Pittler et al.

Electrophoresis, 30(16), 2897-2904 (2009-08-06)

This work deals with the application of silica-based ligand-exchange chiral stationary phases (CSPs) for the enantioseparation of underivatized amino acids, alpha-hydroxy acids, and dipeptides with packed CEC. Two different possibilities of preparing silica-based CSPs are presented. One phase contains L-4-hydroxyproline

Does the anabolic metabolism of L-[2-18F]fluorophenylalanine and L-[2,6-3H]phenylalanine differ in the cerebrum and the cerebellum?

H Nakamichi et al.

Nuclear medicine and biology, 21(7), 959-962 (1994-10-01)

The anabolism of isotopically labeled amino acids was compared between the cerebrum and the cerebellum in conscious rat at three feeding conditions. After L-[2-18F]fluorophenylalanine and L-[2,6-3H]phenylalanine injections, the incorporation rate of both radioactivity into protein fraction showed no difference between

Structure-activity relationships among substituted N-benzoyl derivatives of phenylalanine and its analogs in a microbial antitumor prescreen I: Derivatives of o-fluoro-DL-phenylalanine.

T T Otani et al.

Journal of pharmaceutical sciences, 71(2), 214-216 (1982-02-01)

Twelve derivatives of 0-fluoro-dl-phenylalanine containing fluorine, chlorine, methoxy, and nitro radicals in various positions of the aromatic ring of the benzoyl group were prepared and tested in a Lactobacillus casei system. It was found that most substitutions in the benzoyl

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