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240834

Diphenyl ether

ReagentPlus®, ≥99%

Synonyme(s) :

Diphenyl oxide, Phenyl ether

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A propos de cet article

Formule linéaire :
(C6H5)2O
Numéro CAS:
101-84-8
Poids moléculaire :
170.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24854438
EC Number:
202-981-2
Beilstein/REAXYS Number:
1364620
MDL number:
MFCD00003034
Assay:
≥99%
Bp:
259 °C (lit.)
Vapor pressure:
<1 mmHg ( 20 °C)
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vapor density

>5.86 (25 °C, vs air)

Quality Level

100

vapor pressure

<1 mmHg ( 20 °C)

product line

ReagentPlus®

assay

≥99%

form

crystalline

autoignition temp.

1144 °F

expl. lim.

1.5 %

dilution

(for general lab use)

refractive index

n20/D 1.579 (lit.)

bp

259 °C (lit.)

mp

25-27 °C (lit.)

solubility

alcohol: soluble(lit.), benzene: soluble(lit.), diethyl ether: soluble(lit.), glacial acetic acid: soluble(lit.), water: insoluble(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

The diphenyl derivatives, having potency for inhibiting InhA (an essential enoyl acyl carrier protein reductase involved in mycolic acid biosynthesis), were studied.

Application

Diphenyl ether can be used as:
  • An additive in the fabrication of thienothiophene-co-benzodithiophene polymer-based organic photovoltaics and isoindigo polymer-based organic solar cells.
  • A model compound to study the hydrodeoxygenation of ether linkages in the lignin fragments using various catalytic systems.
  • A solvent in the synthesis of FePd nanoparticles using modified polyol process.

Legal Information

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

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Danger

Hazard Classifications

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

Classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

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Certificats d'analyse (COA)

Lot/Batch Number
SHBT3582
SHBS6993
SHBR4477
SHBR8139
SHBR0573

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P Kamsri et al.
SAR and QSAR in environmental research, 25(6), 473-488 (2014-05-03)
A series of diphenyl ether derivatives were developed and showed promising potency for inhibiting InhA, an essential enoyl acyl carrier protein reductase involved in mycolic acid biosynthesis, leading to the lysis of Mycobacterium tuberculosis. To understand the structural basis of
Hydrodeoxygenation of lignin-derived phenolic compounds over bi-functional Ru/H-Beta under mild conditions
Yao G, et al.
Fuel: The Science and Technology of Fuel and Energy, 150, 175-183 (2015)
Isoindigo-based conjugated polymer for high-performance organic solar cell with a high VOC of 1.06 V as processed from non-halogenated solvent
Jung EH, et al.
Dyes and Pigments, 161, 113-118 (2019)
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