541168
3′,5′-Difluoroacetophenone
97%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
F2C6H3COCH3
CAS Number:
Molecular Weight:
156.13
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
InChI
1S/C8H6F2O/c1-5(11)6-2-7(9)4-8(10)3-6/h2-4H,1H3
SMILES string
CC(=O)c1cc(F)cc(F)c1
InChI key
OXJLDNSPGPBDCP-UHFFFAOYSA-N
assay
97%
mp
34-38 °C (lit.)
functional group
fluoro, ketone
Quality Level
General description
3′,5′-Difluoroacetophenone, also known as 1-(3,5-difluorophenyl)ethanone, is a fluorinated acetophenone.
Application
3′,5′-Difluoroacetophenone (3,5-Difluoroacetophenone) may be used to synthesize:
- (E)-3-(4-(1,5,9-trithia-13-azacyclohexadecan-13-yl)-phenyl)-1-(3,5-difluorophenyl)prop-2-en-1-one
- 1,3,5-triarylpyrazoline fluorophores containing a 16-membered thiazacrown ligand
- (±)-fluorinated-1-(3-morpholin-4-yl-phenyl)ethylamine
- (E)-1-(3,5-difluorophenyl)-3-(2,4-dimethoxyphenyl) prop-2-en-1-one
- 1-(3,5-difluorophenyl)-4,4,4-trifluorobutane-1,3-dione
signalword
Warning
hcodes
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
180.0 °F - closed cup
flash_point_c
82.2 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
(E)-1-(3, 5-Difluorophenyl)-3-(2, 4-dimethoxyphenyl) prop-2-en-1-one.
Huang T, et al.
Acta Crystallographica Section E, Structure Reports Online, 66(10), o2518-o2518 (2010)
1-(3, 5-Difluorophenyl)-4, 4, 4-trifluorobutane-1, 3-dione.
Manoj Kumar KE, et al.
Acta Crystallographica Section E, Structure Reports Online, 69(11), o1705-o1705 (2013)
Yong-Jin Wu et al.
Bioorganic & medicinal chemistry letters, 13(10), 1725-1728 (2003-05-06)
The synthesis of four (+/-)-fluorinated 1-(3-morpholin-4-yl-phenyl)-ethylamines and an enantioselective approach to these amines through reductive amination are described.
Manjusha Verma et al.
Organic & biomolecular chemistry, 8(2), 363-370 (2010-01-13)
We have prepared and characterized a Cu(i)-responsive fluorescent probe, constructed using a large tetradentate, 16-membered thiazacrown ligand ([16]aneNS(3)) and 1,3,5-triaryl-substituted pyrazoline fluorophores. The fluorescence contrast ratio upon analyte binding, which is mainly governed by changes of the photoinduced electron transfer
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service