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P24101

Sigma-Aldrich

Diphenyl ether

ReagentPlus®, 99%

Sinônimo(s):

Diphenyl oxide, Phenyl ether

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About This Item

Fórmula linear:
(C6H5)2O
Número CAS:
101-84-8
Peso molecular:
170.21
Beilstein:
1364620
Número CE:
202-981-2
Número MDL:
MFCD00003034
Código UNSPSC:
12352100
ID de substância PubChem:
57654511
NACRES:
NA.21

densidade de vapor

>5.86 (25 °C, vs air)

Nível de qualidade

200

pressão de vapor

<1 mmHg ( 20 °C)

linha de produto

ReagentPlus®

Ensaio

99%

forma

crystals

temperatura de autoignição

1144 °F

Lim. expl.

1.5 %

índice de refração

n20/D 1.579 (lit.)

pb

259 °C (lit.)

pf

25-27 °C (lit.)

densidade

1.073 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

O(c1ccccc1)c2ccccc2

InChI

1S/C12H10O/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10H

chave InChI

USIUVYZYUHIAEV-UHFFFAOYSA-N

Informações sobre genes

human ... TTR(7276)

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Descrição geral

Diphenyl ether (DPE) is a bridged-phenyl molecule. The conformational analysis of using resonance-enhanced two-photon ionization method DPE has been reported.

Aplicação

Diphenyl ether may be used to synthesize dibenzofuran via intramolecular cyclization in the presence of palladium acetate.

Informações legais

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogramas

Exclamation markEnvironment
GHS07,GHS09

Palavra indicadora

Warning

Frases de perigo

H319,H410

Classificações de perigo

Aquatic Acute 1 - Aquatic Chronic 2 - Eye Irrit. 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

239.0 °F - closed cup

Ponto de fulgor (°C)

115 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificados de análise (COA)

Lot/Batch Number
SDBB0491
MKCV5118
STBL1397
STBK6041
MKCS1080

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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)
Julie B Herbstman et al.
Environmental health perspectives, 115(12), 1794-1800 (2007-12-19)
Recent studies have reported blood levels of polybrominated diphenyl ethers (PBDEs) in the U.S. population. Information about neonatal levels and about the relationship to polychlorinated biphenyls (PCBs) exposures is limited. The objective was to characterize levels and determinants of fetal
Xingyu Wang et al.
ChemSusChem, 5(8), 1455-1466 (2012-05-03)
The conversion of lignin, the most recalcitrant of the biopolymers, is necessary for a carbon-efficient utilization of lignocellulosic materials. In this context, hydrogenolysis of lignin is a process receiving increasing attention. In this report, the solvent effects on the hydrogenolysis
Sindra L Summoogum et al.
Chemosphere, 85(2), 143-150 (2011-07-09)
This article examines the thermal decomposition of alpha-cypermethrin, one of the most common pyrethroid pesticides. The objective was to identify its decomposition pathways and to gain an understanding into the formation of toxic species in the environment, including those that
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