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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-(4-chloropyrimidin-2-yl)piperazine-1-carboxylate

Clc1ccnc(n1)N1CCN(CC1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 4-(4-chloropyrimidin-2-yl)piperazine-1-carboxylate
CAS Number: 479691-42-4
Product Number: AG00DCT2(AGN-PC-07XTIJ)
Synonyms:
MDL No:
Molecular Formula: C13H19ClN4O2
Molecular Weight: 298.7686

Identification/Properties

Computed Properties
Molecular Weight:
298.771g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
298.12g/mol
Monoisotopic Mass:
298.12g/mol
Topological Polar Surface Area:
58.6A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
340
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 4-(4-chloropyrimidin-2-yl)piperazine-1-carboxylate is a versatile chemical compound commonly used in chemical synthesis processes. It serves as a key building block for the creation of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties and reactivity. In chemical synthesis, this compound can be utilized as a critical intermediary in the formation of complex organic molecules, enabling the introduction of specific functional groups and enhancing the overall efficiency of the synthesis pathways. Additionally, the tert-Butyl 4-(4-chloropyrimidin-2-yl)piperazine-1-carboxylate demonstrates excellent compatibility with a wide range of other reagents and substrates, making it a valuable tool for chemists and researchers seeking to develop novel compounds with tailored properties and applications.