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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)-

1,3-Piperazinedicarboxylic acid, 1-(1,1-dimethylethyl) 3-ethyl ester

CCOC(=O)C1NCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1,3-Piperazinedicarboxylic acid, 1-(1,1-dimethylethyl) 3-ethyl ester
CAS Number: 183742-29-2
Product Number: AG00AMNJ(AGN-PC-008ED8)
Synonyms:
MDL No:
Molecular Formula: C12H22N2O4
Molecular Weight: 258.3141

Identification/Properties

Computed Properties
Molecular Weight:
258.318g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
5
Exact Mass:
258.158g/mol
Monoisotopic Mass:
258.158g/mol
Topological Polar Surface Area:
67.9A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
312
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


1-tert-Butyl 3-ethyl piperazine-1,3-dicarboxylate, commonly referred to as $name$, is a versatile compound that finds significant application in chemical synthesis. This compound serves as a key building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. In chemical synthesis, $name$ acts as a valuable intermediate in the preparation of complex organic molecules due to its unique structural characteristics and reactivity profile. Its tert-butyl and ethyl substituents, combined with the piperazine and dicarboxylate moieties, impart specific chemical properties that enable it to participate in a wide range of synthetic transformations. These include reactions such as acylation, alkylation, and cyclization, making it a valuable tool for creating diverse molecular structures with tailored properties. Additionally, the presence of the piperazine ring in $name$ confers the potential for chirality, further widening its applicability in asymmetric synthesis processes. Overall, the versatility and reactivity of 1-tert-Butyl 3-ethyl piperazine-1,3-dicarboxylate make it a valuable asset in the realm of chemical synthesis, facilitating the creation of novel compounds with promising applications in various fields.