264466
2,6-Difluorophenol
98%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
F2C6H3OH
CAS Number:
Molecular Weight:
130.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
248-884-9
Beilstein/REAXYS Number:
2043613
MDL number:
Assay:
98%
Form:
solid
InChI key
CKKOVFGIBXCEIJ-UHFFFAOYSA-N
InChI
1S/C6H4F2O/c7-4-2-1-3-5(8)6(4)9/h1-3,9H
SMILES string
Oc1c(F)cccc1F
assay
98%
form
solid
storage condition
protect from light
bp
59-61 °C/17 mmHg (lit.)
mp
38-41 °C (lit.)
solubility
ethanol: soluble 50 mg/mL, clear, colorless to light yellow
functional group
fluoro
storage temp.
2-8°C
Quality Level
Application
2,6-difluorophenol undergoes oxidative polymerization in the presence of the Fe-N,N′-bis(salicylidene)ethylenediamine (salen) complex (catalyst) and hydrogen peroxide (oxidizing agent) to give poly(2,6-difluoro-1,4-phenylene oxide).
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Sol. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
4.1B - Flammable solid hazardous materials
wgk
WGK 3
flash_point_f
136.4 °F - closed cup
flash_point_c
58 °C - closed cup
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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.
J Qiu et al.
Journal of medicinal chemistry, 42(2), 329-332 (1999-02-02)
3-(Aminomethyl)-2,6-difluorophenol (6) and 4-(aminomethyl)-2, 6-difluorophenol (7) were synthesized in eight and four steps, respectively, starting from 2,6-difluorophenol, to test the potential of the 2,6-difluorophenol moiety to act as a lipophilic bioisostere of a carboxylic acid. Compounds 6 and 7 are
Oxidative Polymerization of 2,6-Difluorophenol to Crystalline Poly(2,6-difluoro-1,4-phenylene oxide).
Ikeda R, et al.
Macromolecules, 33(18), 6648-6652 (2000)
Jiasong Li et al.
Biochemistry, 58(17), 2218-2227 (2019-04-05)
Cysteine dioxygenase (CDO) is a nonheme iron enzyme that adds two oxygen atoms from dioxygen to the sulfur atom of l-cysteine. Adjacent to the iron site of mammalian CDO, there is a post-translationally generated Cys-Tyr cofactor, whose presence substantially enhances
Akira Ohashi et al.
Talanta, 146, 789-794 (2015-12-24)
The solubilities of several cobalt(III) chelates (CoL3) with in supercritical carbon dioxide (SC-CO2) were investigated in the presence of fluorine- and trifluoromethyl-substituted phenols (PhOH) using UV-vis spectrophotometry. Solubility enhancement of CoL3 complexes in SC-CO2 was accomplished by adding PhOH. The
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