Skip to Content
MilliporeSigma
All Photos(2)

Key Documents

View All Documentation

193011

Sigma-Aldrich

2-Furaldehyde diethyl acetal

97%

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Empirical Formula (Hill Notation):
C9H14O3
CAS Number:
13529-27-6
Molecular Weight:
170.21
EC Number:
236-872-6
MDL number:
MFCD00003245
UNSPSC Code:
12352100
PubChem Substance ID:
24851576
NACRES:
NA.22

assay

97%

form

liquid

refractive index

n20/D 1.444 (lit.)

bp

189-191 °C (lit.)

density

1.008 g/mL at 25 °C (lit.)

functional group

ether

SMILES string

CCOC(OCC)c1ccco1

InChI

1S/C9H14O3/c1-3-10-9(11-4-2)8-6-5-7-12-8/h5-7,9H,3-4H2,1-2H3

InChI key

SEILDMUKBMYIEZ-UHFFFAOYSA-N

Application

2-Furaldehyde diethyl acetal was used in the synthesis of:
  • 5-pyridyl- and 5-aryl-2-furaldehydes via Palladium-mediated cross-coupling reaction[1]
  • 11-oxatricyclo [5.3. 1.02, 6] undecane derivatives[2]

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

147.2 °F - closed cup

flash_point_c

64 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
02907EH
12626AI
09808LU
09222HI
12030LU

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Donald R Gauthier et al.
Organic letters, 4(3), 375-378 (2002-02-01)
5-Pyridyl- and 5-aryl-2-furaldehydes are prepared from furaldehyde diethyl acetal in a four-step, one-pot procedure:(i) deprotonation; (2) Li to Zn transmetalation; (3) Pd-mediated cross-coupling; (4) aldehyde deprotection. Triorganozincate 7 was found to transfer all three groups in the Pd-catalyzed cross-coupling reaction
Synthesis of 11-oxatricyclo [5.3. 1.02, 6] undecane derivatives via organometallic cyclizations.
La Belle BE, et al.
The Journal of Organic Chemistry, 50(25), 5215-5222 (1985)
Vijayakumar Karuppiah et al.
World journal of microbiology & biotechnology, 37(4), 66-66 (2021-03-20)
Pseudomonas aeruginosa is one of the vulnerable opportunistic pathogens associated with nosocomial infections, cystic fibrosis, burn wounds and surgical site infections. Several studies have reported that quorum sensing (QS) systems are controlled the P. aeruginosa pathogenicity. Hence, the targeting of

Questions

Reviews

No rating value

Active Filters

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