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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)-

6-[4-(2-piperidin-1-ylethoxy)phenyl]-3-pyridin-4-ylpyrazolo[1,5-a]pyrimidine;dihydrochloride

C1CCN(CC1)CCOc1ccc(cc1)c1cnc2n(c1)ncc2c1ccncc1.Cl.Cl Request for Quotation
Chemical Name: 6-[4-(2-piperidin-1-ylethoxy)phenyl]-3-pyridin-4-ylpyrazolo[1,5-a]pyrimidine;dihydrochloride
CAS Number: 1219168-18-9
Product Number: AG0016E6(AGN-PC-086G1K)
Synonyms:
MDL No: MFCD11112197
Molecular Formula: C24H27Cl2N5O
Molecular Weight: 472.4101

Identification/Properties

Computed Properties
Molecular Weight:
472.414g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
6
Exact Mass:
471.159g/mol
Monoisotopic Mass:
471.159g/mol
Topological Polar Surface Area:
55.6A^2
Heavy Atom Count:
32
Formal Charge:
0
Complexity:
514
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:
3
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The Pyrazolo[1,5-a]pyrimidine, 6-[4-[2-(1-piperidinyl)ethoxy]phenyl]-3-(4-pyridinyl)-, hydrochloride (1:2) compound serves a crucial role in chemical synthesis processes. Specifically, its application is instrumental in the development of novel pharmaceuticals, agrochemicals, and materials due to its unique structural properties and reactivity.This compound can be utilized as a key intermediate in the synthesis of various biologically active molecules and therapeutic agents. Its specific chemical structure enables it to participate in diverse reaction mechanisms, leading to the formation of complex molecular architectures with desired properties.Moreover, the hydrochloride salt form of this compound enhances its solubility and stability, making it more convenient for use in chemical reactions. By incorporating this compound into synthetic routes, chemists can access a wide range of structurally diverse compounds that possess potential applications in fields such as medicine, agriculture, and materials science.