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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)-

4-Piperidinol, 1-(2-chloro-4-pyrimidinyl)-

OC1CCN(CC1)c1ccnc(n1)Cl Request for Quotation
Chemical Name: 4-Piperidinol, 1-(2-chloro-4-pyrimidinyl)-
CAS Number: 94222-07-8
Product Number: AG00GVEO(AGN-PC-00M502)
Synonyms:
MDL No:
Molecular Formula: C9H12ClN3O
Molecular Weight: 213.6641

Identification/Properties

Computed Properties
Molecular Weight:
213.665g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
213.067g/mol
Monoisotopic Mass:
213.067g/mol
Topological Polar Surface Area:
49.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
185
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 1-(2-Chloropyrimidin-4-yl)-4-piperidinol compound plays a crucial role in chemical synthesis as a versatile building block. It is commonly utilized as a key intermediate in the pharmaceutical industry for the synthesis of various drugs and pharmacologically active compounds. Its unique chemical structure allows for the introduction of diverse functional groups and modifications, making it an essential component in the development of new therapeutic agents. Additionally, the compound's reactivity and compatibility with a wide range of coupling reactions enable chemists to access a myriad of complex molecular structures efficiently. Its significance in medicinal chemistry and drug discovery processes highlights its importance as a valuable tool for synthetic chemists seeking to create novel drug candidates and biologically active molecules.