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Merck
CN

196398

Furan-3-methanol

99%

Synonym(s):

3-(Hydroxymethyl)furan

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About This Item

Empirical Formula (Hill Notation):
C5H6O2
CAS Number:
Molecular Weight:
98.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-570-7
Beilstein/REAXYS Number:
106456
MDL number:
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Product Name

Furan-3-methanol, 99%

InChI key

STJIISDMSMJQQK-UHFFFAOYSA-N

InChI

1S/C5H6O2/c6-3-5-1-2-7-4-5/h1-2,4,6H,3H2

SMILES string

OCc1ccoc1

assay

99%

form

liquid

refractive index

n20/D 1.484 (lit.)

bp

79-80 °C/17 mmHg (lit.)

density

1.139 g/mL at 25 °C (lit.)

functional group

hydroxyl

Quality Level

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Application

Furan-3-methanol was used in the synthesis of substituted δ2-butenolides and 1-benzyl-3-(furan-3-ylmethyl)-3-methylpyrrolidin-2-one.

General description

Furan-3-methanol on oxidation with pyridinium chlorochromate yields furan-3-carboxaldehyde.

pictograms

FlameExclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

100.4 °F - closed cup

flash_point_c

38 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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3-Alkylfurans as useful synthetic equivalents for substituted δ2-butenolides.
Goldsmith D, et al.
Tetrahedron Letters, 24(52), 5835-5838 (1983)
Stannylation/destannylation. Preparation of. alpha.-alkoxy organolithium reagents and synthesis of dendrolasin via a carbinyl carbanion equivalent.
Still WC.
Journal of the American Chemical Society, 100(5), 1481-1487 (1978)
Jai K Chavda et al.
European journal of organic chemistry, 2014(1), 129-139 (2014-05-16)
The tricyclic BCD substructure of the marine natural product nakadomarin A has been synthesised. The strategy utilised a key carbon-carbon bond-forming reaction between a furan and an

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