Skip to Content
MilliporeSigma
All Photos(3)

Documents

200018

Sigma-Aldrich

2,3-Dihydrofuran

99%

Synonym(s):

2,3-DHF

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Empirical Formula (Hill Notation):
C4H6O
CAS Number:
1191-99-7
Molecular Weight:
70.09
Beilstein/REAXYS Number:
103168
EC Number:
214-747-7
MDL number:
MFCD00003205
UNSPSC Code:
12352100
PubChem Substance ID:
24851953
NACRES:
NA.22

vapor pressure

14.46 psi ( 55 °C)
3.67 psi ( 20 °C)

Quality Level

100

assay

99%

form

liquid

refractive index

n20/D 1.423 (lit.)

bp

54-55 °C (lit.)

density

0.927 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

C1CC=CO1

InChI

1S/C4H6O/c1-2-4-5-3-1/h1,3H,2,4H2

InChI key

JKTCBAGSMQIFNL-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

The enantioselective Heck arylation of 2,3-dihydrofuran with aryl iodides was studied.

Application

2,3-Dihydrofuran is a versatile reagent used in lanthanide-catalyzed Diels-Alder reactions with 2-pyrones and in Rh(II)-stabilized cycloadditions with vinylcarbenoids.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

supp_hazards

EUH019

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

-11.2 °F - closed cup

flash_point_c

-24 °C - closed cup

ppe

Eyeshields, Faceshields, 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

Claudia G Cobo-Angel et al.
Scientific reports, 9(1), 14025-14025 (2019-10-03)
Group B Streptococcus (GBS), is a leading cause of neonatal death and an emerging pathogen in adults. Additionally, GBS is a bovine pathogen causing intramammary infections. The likelihood of GBS interspecies transmission is largely unknown. We explored the potential transmission
Tetrahedron, 50, 4557-4557 (1994)
Synlett, 431-431 (1994)
The Journal of Organic Chemistry, 59, 4535-4535 (1994)
Angela M Bernard et al.
Organic letters, 7(21), 4565-4568 (2005-10-08)
[reactions: see text] Regioselective synthesis of 2,4,5- or 3,4,5-trisubstituted 2,3-dihydrofurans has been realized by using donor-acceptor cyclopropanes or by a Corey ylide reaction with alpha-sulfenyl-, alpha-sulfinyl-, or alpha-sulfonylenones. The method allowed a straightforward synthesis of the natural product calyxolane B.
View All Related Papers

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