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F13304

4-Fluorophenylacetic acid

Name: 4-Fluorophenylacetic acid
Brand: ALDRICH

98%

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About This Item

Fórmula lineal:

FC₆H₄CH₂CO₂H

Número de CAS:

405-50-5

Peso molecular:

154.14

Beilstein/REAXYS Number:

972145

EC Number:

206-972-4

MDL number:

MFCD00004343

UNSPSC Code:

12352100

PubChem Substance ID:

24894761

NACRES:

NA.22

assay

98%

mp

81-83 °C (lit.)

SMILES string

OC(=O)Cc1ccc(F)cc1

InChI

1S/C8H7FO2/c9-7-3-1-6(2-4-7)5-8(10)11/h1-4H,5H2,(H,10,11)

InChI key

MGKPFALCNDRSQD-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

117714

3-Methoxybenzoic acid

Sigma-Aldrich

P16621

Phenylacetic acid

Investigations into tumor accumulation and peroxisome proliferator activated receptor binding by F-18 and C-11 fatty acids.

Stephanie D Jonson et al.

Nuclear medicine and biology, 29(2), 211-216 (2002-02-02)

[11C]Acetate, a myocardial PET imaging agent for analysis of oxidative metabolism, has potential use in tumor imaging. Aromatic fatty acids display antitumor effects with phenylacetate currently in clinical trial. Tumor differentiation and cytostasis resulting from phenylacetate treatment may involve the

Chromatographic selectivity study of 4-fluorophenylacetic acid positional isomers separation.

Tyson Chasse et al.

Journal of chromatography. A, 1156(1-2), 25-34 (2007-06-06)

Unique properties of the fluorine atom stimulate widespread use and development of new organofluorine compounds in agrochemistry, biotechnology and pharmacology applications. However, relatively few synthetic methods exhibit a high degree of fluorination selectivity, which ultimately results in the presence of

Transfer of parahydrogen-induced hyperpolarization to 19F.

Lars T Kuhn et al.

The journal of physical chemistry. A, 110(10), 3521-3526 (2006-03-11)

Homogeneous hydrogenations of unsaturated substrates with parahydrogen yield strong NMR signal enhancements of the transferred 1H nuclei if the symmetry of H2 is broken in the resulting hydrogenated products. This chemically induced hyperpolarization known as Parahydrogen-induced polarization (PHIP) is also

Glucosamine-Based Supramolecular Nanotubes for Human Mesenchymal Cell Therapy.

Satish Kumar Talloj et al.

ACS applied materials & interfaces, 10(17), 15079-15087 (2018-04-14)

Herein, we demonstrate an example of glucosamine-based supramolecular hydrogels that can be used for human mesenchymal cell therapy. We designed and synthesized a series of amino acid derivatives based on a strategy of capping d-glucosamine moiety at the C-terminus and

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