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Merck
CN

290440

3,5-Difluorophenylacetic acid

99%

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About This Item

Linear Formula:
F2C6H3CH2CO2H
CAS Number:
Molecular Weight:
172.13
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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InChI

1S/C8H6F2O2/c9-6-1-5(3-8(11)12)2-7(10)4-6/h1-2,4H,3H2,(H,11,12)

SMILES string

OC(=O)Cc1cc(F)cc(F)c1

InChI key

IGGNSAVLXJKCNH-UHFFFAOYSA-N

assay

99%

mp

68-70 °C (lit.)

General description

3,5-Difluorophenylacetic acid is an important pharmaceutical intermediate.

Application

3,5-Difluorophenylacetic acid has been used in the synthesis of:
  • N-[N-(3,5-difluorophenylacetyl)-L-alanyl]-L-phenylglycine tert-butyl ester
  • N-acylalanine

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Gilles Quéléver et al.
Organic & biomolecular chemistry, 3(13), 2450-2457 (2005-06-25)
Inhibition of gamma-secretase, one of the enzymes responsible for the cleavage of the amyloid precursor protein (APP) to produce pathogenic Abeta peptides, is an attractive approach for the treatment of Alzheimer's disease. We designed a gamma-secretase inhibitor bearing an ascorbic
Synthesis of a tetrahydroimidazo [2', 1': 2, 3] thiazolo [5, 4-c] pyridine derivative with Met inhibitory activity.
Amat M, et al.
ARKIVOC (Gainesville, FL, United States), 3, 145-151 (2010)
Synthesis of dihalophenylacetic acids using aromatic nucleophilic substitution strategy.
Kowalczyk BA.
Synthesis, 1997(12), 1411-1414 (1997)

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