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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)-

Isoxazolo[5,4-b]pyridin-3-amine

Nc1noc2c1cccn2 Request for Quotation
Chemical Name: Isoxazolo[5,4-b]pyridin-3-amine
CAS Number: 92914-74-4
Product Number: AG006K9J(AGN-PC-0KKPPU)
Synonyms:
MDL No:
Molecular Formula: C6H5N3O
Molecular Weight: 135.1234

Identification/Properties

Properties
MP:
212-214 °C
BP:
336.6°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
135.126g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
135.043g/mol
Monoisotopic Mass:
135.043g/mol
Topological Polar Surface Area:
64.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
130
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


Isoxazolo[5,4-b]pyridin-3-amine, a versatile heterocyclic compound, serves as a crucial building block in chemical synthesis. This unique molecule finds application in a range of organic reactions, offering a valuable platform for creating diverse molecular structures. Its presence in synthetic chemistry enables the formation of novel pharmaceuticals, agrochemicals, and materials with enhanced properties. By participating in various transformations such as cross-coupling reactions, cyclizations, and functional group modifications, Isoxazolo[5,4-b]pyridin-3-amine contributes significantly to the development of innovative compounds with potential industrial and medicinal applications.