Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

198242

Sigma-Aldrich

Tetrahydro-4H-pyran-4-one

99%

Synonym(s):

4-Oxotetrahydropyran

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

About This Item

Empirical Formula (Hill Notation):
C5H8O2
CAS Number:
29943-42-8
Molecular Weight:
100.12
Beilstein:
106463
EC Number:
249-967-2
MDL number:
MFCD00006581
UNSPSC Code:
12352100
PubChem Substance ID:
24851869
NACRES:
NA.22

Assay

99%

form

liquid

refractive index

n20/D 1.452 (lit.)

bp

166-166.5 °C (lit.)

density

1.084 g/mL at 25 °C (lit.)

functional group

ether

SMILES string

O=C1CCOCC1

InChI

1S/C5H8O2/c6-5-1-3-7-4-2-5/h1-4H2

InChI key

JMJRYTGVHCAYCT-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Pictograms

Flame
GHS02

Signal Word

Warning

Hazard Statements

H226

Precautionary Statements

P210

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

131.0 °F - closed cup

Flash Point(C)

55 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCC6559
BCCB4395
BCBT1417
BCBQ6678V
MKBP6938V

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

R K Anderson et al.
The Journal of antibiotics, 46(2), 331-342 (1993-02-01)
Syntheses are described for penicillins (4b approximately 4i, 5a and 5b) which possess a 6 beta-(2-heteroaryl-3-substituted)-propenamido side-chain of fixed geometry. In vitro results for these compounds against a range of Gram-positive and Gram-negative bacteria showed in most cases good stability
Kun Huang et al.
The Journal of organic chemistry, 71(21), 8320-8323 (2006-10-10)
As the first example for the synthesis of optically active alpha-hydroxyaldehydes and alpha-hydroxyketones in ionic liquids, we applied RTILs into L-proline catalyzed direct enantioselective alpha-aminoxylation of both aldehydes and ketones successfully. This protocol features a number of advantages, such as
Synthesis, 672-672 (1994)
Journal of Heterocyclic Chemistry, 31, 397-397 (1994)
Bryan Ringstrand et al.
Beilstein journal of organic chemistry, 7, 386-393 (2011-04-23)
The methodology to prepare 3-substituted 1,5-dibromopentanes I and their immediate precursors, which include 3-substituted 1,5-pentanediols VII or 4-substituted tetrahydropyrans VIII, is surveyed. Such dibromides I are important intermediates in the preparation of liquid crystalline derivatives containing 6-membered heterocyclic rings. Four
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