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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)-

5-(4-amino-1-propan-2-ylpyrazolo[3,4-d]pyrimidin-3-yl)-1,3-benzoxazol-2-amine

Nc1oc2c(n1)cc(cc2)c1nn(c2c1c(N)ncn2)C(C)C Request for Quotation
Chemical Name: 5-(4-amino-1-propan-2-ylpyrazolo[3,4-d]pyrimidin-3-yl)-1,3-benzoxazol-2-amine
CAS Number: 1224844-38-5
Product Number: AG0017AM(AGN-PC-07CHHO)
Synonyms:
MDL No: MFCD22124893
Molecular Formula: C15H15N7O
Molecular Weight: 309.3259

Identification/Properties

Computed Properties
Molecular Weight:
309.333g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
2
Exact Mass:
309.134g/mol
Monoisotopic Mass:
309.134g/mol
Topological Polar Surface Area:
122A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
436
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


3-(2-Amino-5-benzoxazolyl)-1-(1-methylethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. In organic synthesis, this compound serves as a valuable building block for the construction of various complex molecules. Its functional groups enable it to participate in a wide range of chemical reactions, such as nucleophilic substitution, oxidative coupling, and cyclization reactions. Moreover, the presence of the benzoxazole ring and the pyrazolopyrimidine core in this compound provides opportunities for diversification through further derivatization. Researchers and chemists often use this compound as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Overall, the application of 3-(2-Amino-5-benzoxazolyl)-1-(1-methylethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine in chemical synthesis offers a pathway to access structurally diverse compounds with potential biological activities and industrial applications.