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Key Documents

556033

Sigma-Aldrich

Ethyl 4-quinazolone-2-carboxylate

97%

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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.)

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

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’.

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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)

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