All Photos(1)
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
Recommended Products
Quality Level
Assay
97%
mp
189-193 °C (lit.)
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
Related Categories
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
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.
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