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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)-

tert-butyl 4-(5-bromo-4-methylpyridin-2-yl)piperazine-1-carboxylate

O=C(N1CCN(CC1)c1ncc(c(c1)C)Br)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 4-(5-bromo-4-methylpyridin-2-yl)piperazine-1-carboxylate
CAS Number: 944582-92-7
Product Number: AG005WXN(AGN-PC-02MPHM)
Synonyms:
MDL No:
Molecular Formula: C15H22BrN3O2
Molecular Weight: 356.2581

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
356.264g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
355.09g/mol
Monoisotopic Mass:
355.09g/mol
Topological Polar Surface Area:
45.7A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
364
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 4-(5-bromo-4-methylpyridin-2-yl)piperazine-1-carboxylate molecule serves as a versatile building block in chemical synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, which combines a piperazine ring with a pyridine moiety, offers a diverse range of reactivity that can be harnessed to introduce specific functional groups or structural motifs into target molecules. This compound can be utilized as a key intermediate in the synthesis of bioactive compounds, enabling chemists to access a variety of complex structures with potential therapeutic or pesticidal properties. The incorporation of tert-butyl and ester moieties provides stability and facilitates purification processes during the synthesis of valuable compounds. By strategically incorporating tert-Butyl 4-(5-bromo-4-methylpyridin-2-yl)piperazine-1-carboxylate into chemical reactions, researchers can streamline the development of novel compounds with optimized properties for various applications.