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线性分子式:
F2C6H3CH2CO2H
化学文摘社编号:
分子量:
172.13
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
assay
99%
mp
68-70 °C (lit.)
SMILES string
OC(=O)Cc1cc(F)cc(F)c1
InChI
1S/C8H6F2O2/c9-6-1-5(3-8(11)12)2-7(10)4-6/h1-2,4H,3H2,(H,11,12)
InChI key
IGGNSAVLXJKCNH-UHFFFAOYSA-N
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
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)
