Dibenzofuran, 98%, Thermo Scientific Chemicals
Dibenzofuran, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Dibenzofuran, 98%, Thermo Scientific Chemicals

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Quantity:
25 g
100 g
Catalog number A16521.14
also known as A16521-14
Price (USD)/ Each
87.10
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Quantity:
25 g
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Price (USD)/ Each
87.10
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Dibenzofuran, 98%, Thermo Scientific Chemicals
Catalog numberA16521.14
Price (USD)/ Each
87.10
-
Add to cart
Chemical Identifiers
CAS132-64-9
IUPAC Name8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene
Molecular FormulaC12H8O
InChI KeyTXCDCPKCNAJMEE-UHFFFAOYSA-N
SMILESO1C2=C(C=CC=C2)C2=C1C=CC=C2
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SpecificationsSpecification SheetSpecification Sheet
Identification (FTIR)Conforms (non-U.S. specification)
Appearance (Color)White to cream
Assay (GC)≥97.5%
CommentSpecification differs for U.S. and non-U.S. material where indicated
Melting Point (clear melt)79.0-85.0°C
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Applications for GC (Gas Chromatography) and LC (Liquid Chromatography) Analysis. Dibenzofuran as the model substrate in culture procedures.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Applications for GC (Gas Chromatography) and LC (Liquid Chromatography) Analysis. Dibenzofuran as the model substrate in culture procedures.

Solubility
Insoluble in wate(<1mg/mL). Soluble in nonpolar organic solvents.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Peter Fortnagel,; Hauke Harms,; Rolf-Michael Wittich,; Sabine Krohn,; Holger Meyer,; Volker Sinnwell,; Heinz Wilkes,; Wittko Francke.Lithiation with n-BuLi occurs at the 4-position (ortho to the O atom). The 4-lithio derivative has been silylated and a second metallation effected at the 6- (second ortho) position, using n-BuLi and TMEDA, as a route to 4,6-disubstituted derivatives. J. Org. Chem. 1997 , 622259.
  2. Peter Fortnagel,; Hauke Harms,; Rolf-Michael Wittich,; Sabine Krohn,; Holger Meyer,; Volker Sinnwell,; Heinz Wilkes,; Wittko Francke.Metabolism of dibenzofuran by Pseudomonas sp. strain HH69 and the mixed culture HH27. Appl. Environ. Microbiol. 1990 56(4),1148-1156.
  3. Lithiation with n-BuLi occurs at the 4-position (ortho to the O atom). The 4-lithio derivative has been silylated and a second metallation effected at the 6- (second ortho) position, using n-BuLi and TMEDA, as a route to 4,6-disubstituted derivatives: J. Org. Chem., 62, 2259 (1997).