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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)-

2-Benzofurancarboxylic acid, 5-amino-, ethyl ester

CCOC(=O)c1cc2c(o1)ccc(c2)N Request for Quotation
Chemical Name: 2-Benzofurancarboxylic acid, 5-amino-, ethyl ester
CAS Number: 174775-48-5
Product Number: AG001ZY5(AGN-PC-0MUBZ8)
Synonyms:
MDL No:
Molecular Formula: C11H11NO3
Molecular Weight: 205.2099

Identification/Properties

Computed Properties
Molecular Weight:
205.213g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
205.074g/mol
Monoisotopic Mass:
205.074g/mol
Topological Polar Surface Area:
65.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
244
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 5-aminobenzofuran-2-carboxylate is a versatile compound widely used in chemical synthesis. This compound serves as a building block in the creation of various organic molecules due to its unique structure and reactivity. In chemical synthesis, Ethyl 5-aminobenzofuran-2-carboxylate can be utilized as a key intermediate for the production of pharmaceuticals, agrochemicals, and materials with specific properties. Its functionality as both an amine and an ester allows for diverse functional group transformations, making it a valuable tool for the creation of complex organic compounds. Additionally, the presence of the benzofuran ring imparts unique aromatic and electronic properties to the molecule, which can be exploited in the design of novel organic compounds with tailored characteristics. Thus, Ethyl 5-aminobenzofuran-2-carboxylate plays a crucial role in the development of new molecules with targeted applications in various industries.