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Merck

P24101

Diphenyl ether

99%, crystals, ReagentPlus®

동의어(들):

Diphenyl oxide, Phenyl ether

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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
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제품 이름

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

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

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



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문서 라이브러리 방문



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