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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)-

Furo[2,3-b]pyridine-2-carboxylic acid, 3-hydroxy-, ethyl ester

CCOC(=O)c1oc2c(c1O)cccn2 Request for Quotation
Chemical Name: Furo[2,3-b]pyridine-2-carboxylic acid, 3-hydroxy-, ethyl ester
CAS Number: 109274-83-1
Product Number: AG009TMR(AGN-PC-0AALA0)
Synonyms:
MDL No:
Molecular Formula: C10H9NO4
Molecular Weight: 207.1828

Identification/Properties

Computed Properties
Molecular Weight:
207.185g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
207.053g/mol
Monoisotopic Mass:
207.053g/mol
Topological Polar Surface Area:
72.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
246
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 3-hydroxyfuro[2,3-b]pyridine-2-carboxylate serves as a versatile building block in chemical synthesis, particularly in the creation of complex organic molecules. This compound's unique structure offers an array of functional groups that enable it to participate in various reactions, such as esterification, hydroxylation, and cyclization. Its furo[2,3-b]pyridine core provides a valuable scaffold for the construction of pharmacologically relevant compounds and natural product synthesis. Additionally, the presence of the hydroxy group and carboxylate moiety offers opportunities for further derivatization, making it a valuable intermediate in the production of diverse chemical entities.