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108014

Sigma-Aldrich

Benzyl ether

98%

Sinônimo(s):

Dibenzyl ether

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About This Item

Fórmula linear:
(C6H5CH2)2O
Número CAS:
103-50-4
Peso molecular:
198.26
Beilstein:
1911156
Número CE:
203-118-2
Número MDL:
MFCD00004780
Código UNSPSC:
12352100
ID de substância PubChem:
24846794
NACRES:
NA.22

Ensaio

98%

índice de refração

n20/D 1.561 (lit.)

pb

298 °C (lit.)

pf

1.5-3.5 °C (lit.)

solubilidade

H2O: insoluble
acetone: miscible
chloroform: miscible
diethyl ether: miscible
ethanol: miscible

densidade

1.043 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

C(OCc1ccccc1)c2ccccc2

InChI

1S/C14H14O/c1-3-7-13(8-4-1)11-15-12-14-9-5-2-6-10-14/h1-10H,11-12H2

chave InChI

MHDVGSVTJDSBDK-UHFFFAOYSA-N

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Descrição geral

Benzyl ether is an aromatic ether that is commonly employed as a protecting agent and benzylating agent.

Benzyl ether is a plasticizer for nitrocellulose and a solvent in perfumery.

Aplicação

Benzyl ether was used as an effective GFP friendly tissue clearing medium for mouse brains. It was used in a study to develop a detailed protocol for performing 3D imaging of solvent-cleared organs and its application to various microscopy techniques.

Pictogramas

Exclamation markEnvironment
GHS07,GHS09

Palavra indicadora

Warning

Frases de perigo

H317,H410

Classificações de perigo

Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1B

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

278.6 °F - Pensky-Martens closed cup

Ponto de fulgor (°C)

137 °C - Pensky-Martens closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análise (COA)

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One-pot synthesis of mesoporous ZrPW solid acid catalyst for liquid phase benzylation of anisole
Miao Z, et al.
Catalysis Science & Technology, 4, 838-850 (2014)
Active cobalt catalyst for the cleavage of benzyl ether
Wang B, et al.
The Journal of Organic Chemistry, 76, 9531-9535 (2011)
Adam Kimbrough et al.
Proceedings of the National Academy of Sciences of the United States of America, 117(4), 2149-2159 (2020-01-16)
Alcohol abuse and alcohol dependence are key factors in the development of alcohol use disorder, which is a pervasive societal problem with substantial economic, medical, and psychiatric consequences. Although our understanding of the neurocircuitry that underlies alcohol use has improved
Evaluation of the Genetic Toxicity of Synthetic Chemicals (XIV)-in vitro Chromosomal Aberration Assay with 11 Chemicals in Chinese Hamster Lung Cells.
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Organic & biomolecular chemistry, 10(13), 2528-2533 (2012-03-01)
An application of the classical Ritter reaction for the synthesis of unsymmetrical di and trisubstituted ureas catalyzed by FeCl(3) is described. The protocol is of significant interest in view of the easy availability of precursors, mild reaction conditions employed and
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