2-Furylacetone, 99%

Name: 2-Furylacetone, 99%
SKU: B22171.14

CAS: 6975-60-6 | C7H8O2 | 124.139 g/mol

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25 g

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Catalog number B22171.14

also known as B22171-14

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Quantity:

25 g

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Chemical Identifiers

CAS6975-60-6

IUPAC Name1-(furan-2-yl)propan-2-one

Molecular FormulaC7H8O2

InChI KeyIQOJTGSBENZIOL-UHFFFAOYSA-N

SMILESCC(=O)CC1=CC=CO1

Specifications

Specification Sheet

Appearance (Color)Clear colorless to yellow

Assay (GC)≥98.5%

Refractive Index1.4680-1.4735 @ 20?C

FormLiquid

Identification (FTIR)Conforms

Suitable for fragrance applications.2-Furylacetone is used as the reactant in the synthesis and transformations of furan derivatives

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
Suitable for fragrance applications.2-Furylacetone is used as the reactant in the synthesis and transformations of furan derivatives

Solubility
Soluble in alcohol, triacetin.

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:

Hiroshi Yamaoka,; Ikuhiro Mishima,; Mitsuko Miyamoto,; Terukiyo Hanafusa. The Acid-catalyzed Reaction of the 2-Oxabicyclo[4.1.0]hept-3-en-5-one System: Isomerization from Homo-4-pyrones into 2-Furylacetone Derivatives. Bulletin of the Chemical Society of Japan. 1980, 53 (2), 469-477.
A. Ya. Medne,;N. O. Saldabol. Synthesis and transformations of furan derivatives. Chemistry of Heterocyclic Compounds. 1966, 1 (4), 423-425.