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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-bromo-2-piperidin-4-yloxypyrimidine

Brc1cnc(nc1)OC1CCNCC1 Request for Quotation
Chemical Name: 5-bromo-2-piperidin-4-yloxypyrimidine
CAS Number: 792180-52-0
Product Number: AG00G40Z(AGN-PC-03RQV1)
Synonyms:
MDL No:
Molecular Formula: C9H12BrN3O
Molecular Weight: 258.1151

Identification/Properties

Computed Properties
Molecular Weight:
258.119g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
257.016g/mol
Monoisotopic Mass:
257.016g/mol
Topological Polar Surface Area:
47A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
167
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-2-(piperidin-4-yloxy)pyrimidine is a versatile compound commonly used in chemical synthesis as a building block for various organic reactions. Its unique structure featuring a bromine atom and a piperidin-4-yloxy group imparts specific properties that make it valuable in the creation of novel molecules. This compound is frequently employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals due to its ability to participate in diverse chemical transformations. In particular, the presence of the piperidine moiety enhances the compound's reactivity and selectivity in a range of synthetic processes, making it a crucial component in the production of complex organic compounds. The 5-Bromo-2-(piperidin-4-yloxy)pyrimidine has found wide applications in medicinal chemistry, material science, and drug discovery, facilitating the development of new and innovative products across various industries.