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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)-

Pyrimidine, 2-(4-piperidinyloxy)-, monohydrochloride

N1CCC(CC1)Oc1ncccn1.Cl Request for Quotation
Chemical Name: Pyrimidine, 2-(4-piperidinyloxy)-, monohydrochloride
CAS Number: 412293-92-6
Product Number: AG00CAZ8(AGN-PC-0RQ60J)
Synonyms:
MDL No:
Molecular Formula: C9H14ClN3O
Molecular Weight: 215.6800

Identification/Properties

Computed Properties
Molecular Weight:
215.681g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
215.083g/mol
Monoisotopic Mass:
215.083g/mol
Topological Polar Surface Area:
47A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
142
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:
2
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


The 2-(Piperidin-4-yloxy)pyrimidine hydrochloride plays a crucial role in chemical synthesis as a versatile building block. Its unique molecular structure allows for the efficient modification and construction of complex organic molecules. This compound is commonly utilized as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Additionally, it serves as a valuable precursor in the preparation of various heterocyclic compounds with diverse biological activities. The incorporation of 2-(Piperidin-4-yloxy)pyrimidine hydrochloride in chemical reactions enables the synthesis of novel compounds with potential applications in drug discovery and material science.