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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)-

1-(5-bromopyrimidin-2-yl)piperidin-4-ol

OC1CCN(CC1)c1ncc(cn1)Br Request for Quotation
Chemical Name: 1-(5-bromopyrimidin-2-yl)piperidin-4-ol
CAS Number: 887425-47-0
Product Number: AG00GRHV(AGN-PC-0LEO3B)
Synonyms:
MDL No:
Molecular Formula: C9H12BrN3O
Molecular Weight: 258.1151

Identification/Properties

Computed Properties
Molecular Weight:
258.119g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
257.016g/mol
Monoisotopic Mass:
257.016g/mol
Topological Polar Surface Area:
49.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
177
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


1-(5-Bromopyrimidin-2-yl)piperidin-4-ol is a versatile compound widely used in chemical synthesis as a key intermediate in the pharmaceutical industry. This compound plays a crucial role in the development of various pharmaceutical drugs due to its unique chemical properties and structural features. Its ability to undergo specific reactions and form key bonds makes it an essential building block in the synthesis of biologically active molecules. Additionally, 1-(5-Bromopyrimidin-2-yl)piperidin-4-ol is utilized as a core component in the preparation of various heterocyclic compounds with diverse pharmacological activities. Its presence in the synthesis pathway leads to the creation of novel drug candidates with potential therapeutic benefits. By strategically incorporating this compound into chemical reactions, researchers can access a wide range of structurally complex molecules with enhanced biological properties and improved drug efficacy.