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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]pyridin-5-amine

Nc1cnc2c(c1)cco2 Request for Quotation
Chemical Name: Furo[2,3-b]pyridin-5-amine
CAS Number: 34668-30-9
Product Number: AG00CM0A(AGN-PC-03G6NQ)
Synonyms:
MDL No:
Molecular Formula: C7H6N2O
Molecular Weight: 134.1353

Identification/Properties

Computed Properties
Molecular Weight:
134.138g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
134.048g/mol
Monoisotopic Mass:
134.048g/mol
Topological Polar Surface Area:
52A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
129
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Furo[2,3-b]pyridin-5-amine is a versatile building block in chemical synthesis, often utilized for its unique structural and reactivity properties. This compound serves as a valuable intermediate in the preparation of various heterocyclic compounds, pharmaceuticals, agrochemicals, and materials. Its aromatic furo[2,3-b]pyridine ring system offers opportunities for diverse functionalization and modification, making it a key component in the creation of novel organic molecules. Chemists commonly employ Furo[2,3-b]pyridin-5-amine as a key starting material for the development of new drug candidates, agrochemicals with enhanced bioactivity, and functional materials with tailored properties. Its inclusion in synthetic routes enables the construction of complex molecular architectures, making it a fundamental component in the design and synthesis of biologically active compounds and advanced materials.