P24101
Diphenyl ether
99%, crystals, ReagentPlus®
동의어(들):
Diphenyl oxide, Phenyl ether
조직 및 계약 가격을 보려면 로그인를 클릭합니다.
크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
(C6H5)2O
CAS 번호:
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
제품 이름
Diphenyl ether, ReagentPlus®, 99%
InChI key
USIUVYZYUHIAEV-UHFFFAOYSA-N
InChI
1S/C12H10O/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10H
SMILES string
O(c1ccccc1)c2ccccc2
vapor density
>5.86 (25 °C, vs air)
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.)
Quality Level
Gene Information
human ... TTR(7276)
density
1.073 g/mL at 25 °C (lit.)
functional group
phenoxy
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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
wgk
WGK 2
flash_point_f
239.0 °F - closed cup
flash_point_c
115 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
signalword
Danger
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 2 - Eye Irrit. 2 - Repr. 1B
저장 등급
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
Palladium-promoted cyclization of diphenyl ether, diphenylamine, and related compounds.
Akermark B, et al.
The Journal of Organic Chemistry, 40(9), 1365-1367 (1975)
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)
Takayuki Yonezawa et al.
Bioorganic & medicinal chemistry letters, 21(11), 3248-3251 (2011-05-10)
Osteogenic activity of six diarylheptanoids, acerogenin A (1), (R)-acerogenin B (2), aceroside I (3), aceroside B(1) (4), aceroside III (5) and (-)-centrolobol (6) and two phenolic compounds; (+)-rhododendrol (7) and (+)-cathechin (8), isolated from the stem bark of Acer nikoense
Robert C Hale et al.
Environment international, 29(6), 771-779 (2003-07-10)
North America consumes over half of the world's production of polybrominated diphenyl ether (PBDE) flame retardants. About 98% of global demand for the Penta-BDE mixture, the constituents of which are the most bioaccumulative and environmentally widespread, resides here. However, research
Ariana Beste et al.
The Journal of organic chemistry, 74(7), 2837-2841 (2009-03-06)
Lignin is an abundant natural resource that is a potential source of valuable chemicals. Improved understanding of the pyrolysis of lignin occurs through the study of model compounds for which phenethyl phenyl ether (PhCH(2)CH(2)OPh, PPE) is the simplest example representing
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