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48190

Sigma-Aldrich

(±)-1-(2-Furyl)ethanol

≥99.0% (GC)

Synonym(s):

(±)-α-Methylfuran-2-methanol, (±)-2-Furyl methyl carbinol

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About This Item

Empirical Formula (Hill Notation):
C6H8O2
CAS Number:
4208-64-4
Molecular Weight:
112.13
Beilstein:
107814
EC Number:
224-130-4
MDL number:
MFCD00077775
UNSPSC Code:
12352100
PubChem Substance ID:
57651149
NACRES:
NA.22
Assay:
≥99.0% (GC)

Quality Level

100

Assay

≥99.0% (GC)

contains

~0.05% hydroquinone as stabilizer

refractive index

n20/D 1.479

bp

167-170 °C

density

1.078 g/mL at 20 °C (lit.)

functional group

hydroxyl

storage temp.

2-8°C

SMILES string

CC(O)c1ccco1

InChI

1S/C6H8O2/c1-5(7)6-3-2-4-8-6/h2-5,7H,1H3

InChI key

UABXUIWIFUZYQK-UHFFFAOYSA-N

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General description

(±)-1-(2-Furyl)ethanol [(±)-2-Furyl methyl carbinol] is a furan derivative. The synthesis of 4-hydroxy-2-methylcyclopent-2-en-1-one from 2-furyl methyl carbinol has been reported.

Application

(±)-1-(2-Furyl)ethanol (Racemic 1-(2-furyl)ethanol) may be used in the synthesis of 1-acetoxy-1-[2-furyl]ethan.

Caution

may discolor to brown on storage

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

48190-10ML-F:
48190-BULK-F:
48190-VAR-F:

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Certificates of Analysis (COA)

Lot/Batch Number
BCBT8328
BCBK8194V
011936/1
11936/1

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An Enantioselective Total Synthetic Approach to (+)-Heptemerone G and (+)-Guanacastepene A from 2-Furyl Methyl Carbinol.
Michalak K and Wicha J.
Synlett, 24, 1387-1390 (2013)
A Ghanem et al.
Chirality, 13(2), 118-123 (2001-02-15)
Asymmetric acetylation of racemic 1-(2-furyl)ethanol with the innocuous acyl donor isopropenyl acetate catalyzed by lipases in organic media afforded the chiral alcohol and acetate in high enantiomeric excess (up to 99%). The effect of molecular sieves as well as organic
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The formation of 2-vinylfuran from the corresponding 4-oxo-2-hexenal (OHE, a lipid oxidation product) under the catalysis of amino acid were studied. The effects of amino acids, reaction temperature, reaction time, water content, pH, metallic ions and some food additives on

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