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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-(3-bromopyridin-2-yl)piperazine-1-carboxylate

O=C(N1CCN(CC1)c1ncccc1Br)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 4-(3-bromopyridin-2-yl)piperazine-1-carboxylate
CAS Number: 1187386-01-1
Product Number: AG003UJY(AGN-PC-07XUJU)
Synonyms:
MDL No:
Molecular Formula: C14H20BrN3O2
Molecular Weight: 342.2315

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
342.237g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
341.074g/mol
Monoisotopic Mass:
341.074g/mol
Topological Polar Surface Area:
45.7A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
338
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 4-(3-bromopyridin-2-yl)piperazine-1-carboxylate is a versatile chemical compound widely used in chemical synthesis applications. This compound serves as a key building block in the creation of various complex molecules, making it a valuable tool for synthetic chemists. By incorporating this compound into reactions, researchers can introduce the unique properties of the 3-bromopyridin-2-yl group and the piperazine ring into the final product. This enables them to modify and functionalize molecules in specific ways to achieve desired chemical properties. In addition, the tert-butyl ester group provides stability and protection during synthetic processes, allowing for selective reactions and precise control over the transformation of functional groups. Overall, the tert-Butyl 4-(3-bromopyridin-2-yl)piperazine-1-carboxylate plays a crucial role in the synthesis of new chemical entities with potential applications in pharmaceuticals, materials science, and other fields.