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About This Item
Linear Formula:
(C6H5)2O
CAS Number:
Molecular Weight:
170.21
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
202-981-2
MDL number:
Beilstein/REAXYS Number:
1364620
Assay:
99%
Form:
crystals
Product Name
Diphenyl ether, ReagentPlus®, 99%
vapor density
>5.86 (25 °C, vs air)
Quality Level
vapor pressure
<1 mmHg ( 20 °C)
product line
ReagentPlus®
assay
99%
form
crystals
autoignition temp.
1144 °F
expl. lim.
1.5 %
refractive index
n20/D 1.579 (lit.)
bp
259 °C (lit.)
mp
25-27 °C (lit.)
density
1.073 g/mL at 25 °C (lit.)
functional group
phenoxy
SMILES string
O(c1ccccc1)c2ccccc2
InChI
1S/C12H10O/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10H
InChI key
USIUVYZYUHIAEV-UHFFFAOYSA-N
Gene Information
human ... TTR(7276)
General description
Diphenyl ether (DPE) is a bridged-phenyl molecule. The conformational analysis of using resonance-enhanced two-photon ionization method DPE has been reported.
Application
Diphenyl ether may be used to synthesize dibenzofuran via intramolecular cyclization in the presence of palladium acetate.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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wgk
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flash_point_f
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flash_point_c
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ppe
dust mask type N95 (US), Eyeshields, Gloves
signalword
Danger
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 2 - Eye Irrit. 2 - Repr. 1B
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
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A REMPI investigation of the minimum energy conformations of diphenyl ether.
Paiva ACS, et al.
International Journal of Mass Spectrometry, 221(2), 107-115 (2002)
Palladium-promoted cyclization of diphenyl ether, diphenylamine, and related compounds.
Akermark B, et al.
The Journal of Organic Chemistry, 40(9), 1365-1367 (1975)
Ge-Fei Hao et al.
Journal of computer-aided molecular design, 25(3), 213-222 (2011-01-25)
Protoporphyrinogen oxidase (PPO, EC 1.3.3.4), which has been identified as a significant target for a great family of herbicides with diverse chemical structures, is the last common enzyme responsible for the seventh step in the biosynthetic pathway to heme and


