Skip to Content
Merck
All Photos(1)

Key Documents

556033

Sigma-Aldrich

Ethyl 4-quinazolone-2-carboxylate

97%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C11H10N2O3
CAS Number:
Molecular Weight:
218.21
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

mp

189-193 °C (lit.)

functional group

ester

SMILES string

CCOC(=O)C1=Nc2ccccc2C(=O)N1

InChI

1S/C11H10N2O3/c1-2-16-11(15)9-12-8-6-4-3-5-7(8)10(14)13-9/h3-6H,2H2,1H3,(H,12,13,14)

InChI key

BMCAWNQKVVTNFP-UHFFFAOYSA-N

General description

Ethyl 4-quinazolone-2-carboxylate is a quinazoline derivative. It can be synthesized from anthranilamide and ethyl oxalate.

Application

Ethyl 4-quinazolone-2-carboxylate may be used to synthesize 4-quinazolone-2-carboxylic acid.

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

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

Visit the Document Library

Nonclassical Antimetabolites. X. 1, 2 A Facile Synthesis of 4-Quinazolone-2-carboxylic Acid and the Structure of Bogert's Ammonium Salt.
Baker BR and Almaula PI.
The Journal of Organic Chemistry, 27(12), 4672-4674 (1962)

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