Skip to Content
Merck
All Photos(1)

Documents

196398

Sigma-Aldrich

Furan-3-methanol

99%

Synonym(s):

3-(Hydroxymethyl)furan

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C5H6O2
CAS Number:
4412-91-3
Molecular Weight:
98.10
Beilstein:
106456
EC Number:
224-570-7
MDL number:
MFCD00005352
UNSPSC Code:
12352100
PubChem Substance ID:
24851756
NACRES:
NA.22

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.)

SMILES string

OCc1ccoc1

InChI

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

InChI key

STJIISDMSMJQQK-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

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

Application

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

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

100.4 °F - closed cup

Flash Point(C)

38 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

3-Alkylfurans as useful synthetic equivalents for substituted δ2-butenolides.
Goldsmith D, et al.
Tetrahedron Letters, 24(52), 5835-5838 (1983)
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
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)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service