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Key Documents

F13304

Sigma-Aldrich

4-Fluorophenylacetic acid

98%

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About This Item

Linear Formula:
FC6H4CH2CO2H
CAS Number:
Molecular Weight:
154.14
Beilstein:
972145
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
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
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
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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