Skip to Content
Merck
All Photos(1)

Documents

Safety Information

359475

Sigma-Aldrich

Methyl 2-oxo-2H-pyran-3-carboxylate

98%

Synonym(s):

Methyl 2-pyrone-3-carboxylate

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

About This Item

Empirical Formula (Hill Notation):
C7H6O4
CAS Number:
25991-27-9
Molecular Weight:
154.12
Beilstein:
1424749
EC Number:
247-397-9
MDL number:
MFCD00075443
UNSPSC Code:
12352100
PubChem Substance ID:
24862080
NACRES:
NA.22

Quality Level

200

Assay

98%

form

powder

bp

146-148 °C/0.75 mmHg (lit.)

mp

75-77 °C (lit.)

SMILES string

COC(=O)C1=CC=COC1=O

InChI

1S/C7H6O4/c1-10-6(8)5-3-2-4-11-7(5)9/h2-4H,1H3

InChI key

GJVZWOMUTYNUCE-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Methyl 2-oxo-2H-pyran-3-carboxylate is a cyclic α,β -unsaturated ketone. It activates caspases-3, -8 and -9 weakly in HL-60 cells.

Application

Methyl 2-oxo-2H-pyran-3-carboxylate is suitable reagent used to investigate the series of simple α,β-unsaturated carbonyl compounds for their cytotoxic profiles against oral human normal and tumor cells.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

359475-BULK:
359475-1G:
359475-5G:
359475-VAR:

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

Risa Takeuchi et al.
Anticancer research, 26(5A), 3343-3348 (2006-11-11)
As previously suggested, codeinone (oxidation product of codeine) induces non-apoptotic cell death, characterized by marginal caspase activation and the lack of DNA fragmentation in HL-60 human promyelocytic leukemia cells, which was inhibited by N-acetyl-L-cysteine. Whether, morphinone, an oxidative metabolite of
Tohru Nakayachi et al.
Anticancer research, 24(2B), 737-742 (2004-05-27)
A series of simple alpha, beta-unsaturated carbonyl compounds (1-26) was characterized for their cytotoxic profiles against oral human normal and tumor cells. Several cycloalkenones showed potent cytotoxic activities against human oral squamous cell carcinoma HSC-2 cell line. Among them, 4,4-dimethyl-2-cyclopenten-1-one

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