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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-methoxycarbonylphenyl)piperazine-1-carboxylate

COC(=O)c1ccc(cc1)N1CCN(CC1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 4-(4-methoxycarbonylphenyl)piperazine-1-carboxylate
CAS Number: 158985-36-5
Product Number: AG001R2Y(AGN-PC-0KL7L1)
Synonyms:
MDL No:
Molecular Formula: C17H24N2O4
Molecular Weight: 320.3835

Identification/Properties

Computed Properties
Molecular Weight:
320.389g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
5
Exact Mass:
320.174g/mol
Monoisotopic Mass:
320.174g/mol
Topological Polar Surface Area:
59.1A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
417
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


1-Piperazinecarboxylic acid, 4-[4-(methoxycarbonyl)phenyl]-, 1,1-dimethylethyl ester, commonly known as $name$ in chemical synthesis, serves a crucial role as a versatile building block in the production of various organic compounds. This compound is widely utilized as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, $name$ acts as a valuable precursor for the creation of complex molecular structures due to its unique chemical properties. Its incorporation in the synthesis of pharmaceutical compounds enables the development of new drugs with enhanced therapeutic effects and improved bioavailability. Additionally, $name$ is instrumental in the production of agrochemicals that contribute to agricultural innovation and crop protection.Furthermore, the versatility of $name$ in chemical synthesis extends to the creation of specialty chemicals used in diverse industrial applications. Its ability to participate in various chemical reactions and functional group transformations makes it an indispensable component in the organic synthesis toolbox. Chemists and researchers rely on the reactivity and stability of $name$ to access novel compounds with tailored properties for specific purposes.Overall, the application of 1-Piperazinecarboxylic acid, 4-[4-(methoxycarbonyl)phenyl]-, 1,1-dimethylethyl ester in chemical synthesis is fundamental in driving advancements in pharmaceutical, agricultural, and industrial sectors by enabling the efficient and precise construction of intricate molecular structures essential for the development of innovative products.