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Dibenzyl ether information


Dibenzyl ether
Names
Preferred IUPAC name
1,1′-[Oxybis(methylene)]dibenzene
Identifiers
CAS Number
  • 103-50-4
3D model (JSmol)
  • Interactive image
ChEMBL
  • ChEMBL152299
ChemSpider
  • 21105876
ECHA InfoCard 100.002.835 Edit this at Wikidata
EC Number
  • 203-118-2
PubChem CID
  • 7657
UNII
  • 2O6CNO27RJ
CompTox Dashboard (EPA)
  • DTXSID5025819
InChI
  • InChI=1S/C14H14O/c1-3-7-13(8-4-1)11-15-12-14-9-5-2-6-10-14/h1-10H,11-12H2
    Key: MHDVGSVTJDSBDK-UHFFFAOYSA-N
SMILES
  • C1=CC=C(C=C1)COCC2=CC=CC=C2
Properties
Chemical formula
 C14H14O
Molar mass 198.265 g·mol−1
Appearance colorless liquid
Density 1.043 g/cm3 (20 °C)
Melting point 3.6 °C (38.5 °F; 276.8 K)
Boiling point 298 °C (568 °F; 571 K)
Hazards
GHS labelling:
Pictograms
 GHS07: Exclamation markGHS09: Environmental hazard
Signal word
 Warning
Hazard statements
 H317, H319, H410, H411
Precautionary statements
 P261, P264, P272, P273, P280, P302+P352, P305+P351+P338, P321, P333+P313, P337+P313, P363, P391, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Dibenzylether is the organic compound with the formula (C6H5CH2)2O. It is classified as an ether derived from benzyl alcohol. A colorless, nearly odorless oil, the compound's main use is as a plasticizer. It is prepared by treating benzyl chloride with base.[1]

  1. ^ Friedrich Brühne; Elaine Wright (2007). "Benzyl Alcohol". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a04_001. ISBN 978-3527306732.

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Dibenzyl ether

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the organic compound with the formula (C6H5CH2)2O. It is classified as an ether derived from benzyl alcohol. A colorless, nearly odorless oil, the compound's...

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Benzyl alcohol

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esters and ethers, used in the soap, perfume, and flavor industries. E.g. benzyl benzoate, benzyl salicylate, benzyl cinnamate, dibenzyl ether, benzyl butyl...

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Benzyl chloride

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chloride. Benzyl ethers are often derived from benzyl chloride. Benzyl chloride reacts with aqueous sodium hydroxide to give dibenzyl ether. In organic synthesis...

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Tissue clearing

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tissue with tetrahydrofuran and dichloromethane before clearing it in dibenzyl ether. A year later, in 2013, Chung et al. developed CLARITY, the first approach...

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3DISCO

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GFP-compatible and provided better clearing. As such, tetrahydrofuran (THF) and dibenzyl ether (DBE) were chosen as the best regents for clearing. Based on these findings...

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Silylation

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248. doi:10.15227/orgsyn.074.0248 Nina Gommermann and Paul Knochel "N,N-Dibenzyl-n-[1-cyclohexyl-3-(trimethylsilyl)-2-propynyl]-amine from Cyclohexanecarbaldehyde...

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Benzylamine

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secondary amine groups are acetylated in acetic anhydride. The resulting dibenzyl-substituted intermediate is then reacted with nitronium tetrafluoroborate...

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Kuwajima Taxol total synthesis

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constructed by nucleophilic addition to the aldehyde of 2.1 (scheme 2) with dibenzyl acetal of 2-bromobenzaldehyde 2.2 as its aryllithium. This step is much...

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Silver hyponitrite

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"347. Alkoxy-radicals. Part I. The kinetics of thermal decomposition of dibenzyl hyponitrite in solution". Journal of the Chemical Society (Resumed): 1788...

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List of compounds with carbon number 15

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molecules – C15H14O2 benzoin methyl ether 3524-62-7 C15H14O2 methyl diphenylacetate 3469-00-9 C15H14O3 dibenzyl carbonate 3459-92-5 C15H14O3 fenoprofen...

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List of compounds with carbon number 22

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C22H17F25O2 perfluorododecyl hexylene methacrylate 138245-45-1 C22H18O4 dibenzyl phthalate 523-31-9 C22H19Br2NO3 deltamethrine 62229-77-0 C22H19Cl2NO3 alphamethrin...

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List of compounds with carbon number 14

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acetophenone phenylhydrazone 583-11-9 C14H14N2 naphazoline 835-31-4 C14H14N2O dibenzyl nitrosamine 5336-53-8 C14H14N2O metyrapone 54-36-4 C14H14N4 glyoxalphenylosazone...

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Emily Fortey

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Proc., 13 (1898) 161-2 Fortey, Emily C. Action of light and oxygen on dibenzyl ketone. Chem. Soc. J., 75 (Pt. 2) (1899) 871-3 Richardson, Arthur; Fortey...

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Expanding monomer

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Toshikazu (November 1987). "Synthesis and cationic polymerization of 3,9-dibenzyl-1,5,7,11-tetraoxaspiro[5.5]undecane". Macromolecules. 20 (6): 1416–1419...

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Naturally occurring phenols

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in non-vascular land plants (bryophytes). Dihydrostilbenoids and bis(dibenzyls) can be found in liverworts (Marchantiophyta), for instance, the macrocycles...

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Biphalin

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ATC code None Identifiers IUPAC name (2S,2’S)-N,N’-[(2R,8S,13S,19R)-8,13-Dibenzyl-3,6,9,12,15,18-hexaoxo-4,7,10,11,14,17-hexaazaicosane-2...

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