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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

4H-1-Benzopyran-2-carboxylic acid, 4-oxo-, ethyl ester

CCOC(=O)c1cc(=O)c2c(o1)cccc2 Request for Quotation
Chemical Name: 4H-1-Benzopyran-2-carboxylic acid, 4-oxo-, ethyl ester
CAS Number: 14736-31-3
Product Number: AG001EUO(AGN-PC-0JKJ31)
Synonyms:
MDL No:
Molecular Formula: C12H10O4
Molecular Weight: 218.2054

Identification/Properties

Computed Properties
Molecular Weight:
218.208g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
218.058g/mol
Monoisotopic Mass:
218.058g/mol
Topological Polar Surface Area:
52.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
332
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 4-oxo-4H-chromene-2-carboxylate, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound serves as a crucial building block in the creation of various organic molecules due to its unique structural properties and reactivity.One of the primary applications of Ethyl 4-oxo-4H-chromene-2-carboxylate in chemical synthesis is its role as a key intermediate in the synthesis of complex heterocyclic compounds. By incorporating this compound into organic reactions, chemists can access a wide range of chromene-based derivatives with diverse functionalities and properties.Furthermore, Ethyl 4-oxo-4H-chromene-2-carboxylate can be used as a starting material for the synthesis of pharmaceuticals, agrochemicals, and materials with specific biological activities. Its presence in the chemical synthesis toolkit enables the efficient construction of novel compounds for various industries and research fields.Overall, Ethyl 4-oxo-4H-chromene-2-carboxylate plays a crucial role in advancing the field of chemical synthesis by facilitating the creation of complex organic molecules with tailored properties and functionalities. Its versatility and utility make it a valuable component in the toolbox of synthetic chemists seeking to explore new avenues in organic synthesis.