196606
2,5-Difluoroaniline
99.5%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
F2C6H3NH2
CAS Number:
Molecular Weight:
129.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-690-1
Beilstein/REAXYS Number:
2802549
MDL number:
Assay:
99.5%
InChI key
YNOOQIUSYGWMSS-UHFFFAOYSA-N
InChI
1S/C6H5F2N/c7-4-1-2-5(8)6(9)3-4/h1-3H,9H2
SMILES string
Nc1cc(F)ccc1F
assay
99.5%
Quality Level
bp
176-178 °C (lit.)
mp
11-13 °C (lit.)
density
1.288 g/mL at 25 °C (lit.)
functional group
fluoro
Application
2,5-Difluoroaniline was used in the synthesis of 2,4-di-tert-butyl-6-[(2,5-difluorophenyl)iminomethyl]phenol. It was also used in ultrasound-assisted preparation of 1,4-diazabutadienes.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Skin Sens. 1
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
150.8 °F - closed cup
flash_point_c
66 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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.
Jing-Yu He et al.
Ultrasonics sonochemistry, 18(1), 466-469 (2010-08-28)
An ultrasound-assisted preparation of 1,4-diazabutadienes via smooth condensation of diketones with amines under solvent-free conditions is described. The generality of this method was examined by the synthesized N,N'-diaryl- and N,N'-dialkyl-1,4-diazabutadiene derivatives. In addition to experimental simplicity, the main advantages of
Omer Celik et al.
Acta crystallographica. Section E, Structure reports online, 65(Pt 11), o2786-o2786 (2009-01-01)
In the title Schiff base, C(21)H(25)F(2)NO, the dihedral angle between the aromatic rings is 27.90(5)° and an intramolecular O-H⋯N hydrogen bond occurs. In the crystal, the molecules are linked by C-H⋯O, C-H⋯N and C-H⋯F interactions.
I M Rietjens et al.
Chemico-biological interactions, 94(1), 49-72 (1995-01-01)
The in vivo metabolite patterns of 2,5-difluoroaminobenzene and of its nitrobenzene analogue, 2,5-difluoronitrobenzene, were determined using 19F NMR analysis of urine samples. Results obtained demonstrate significant differences between the biotransformation patterns of these two analogues. For the aminobenzene, cytochrome P450
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