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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-Piperazinecarboxylicacid, 3-ethyl-, 1,1-dimethylethyl ester, (3S)-

CC[C@@H]1NCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1-Piperazinecarboxylicacid, 3-ethyl-, 1,1-dimethylethyl ester, (3S)-
CAS Number: 928025-56-3
Product Number: AG0060SS(AGN-PC-0W1I9L)
Synonyms:
MDL No: MFCD07772110
Molecular Formula: C11H22N2O2
Molecular Weight: 214.3046

Identification/Properties

Properties
BP:
287℃
Storage:
2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
214.309g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
214.168g/mol
Monoisotopic Mass:
214.168g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
223
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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


(S)-tert-Butyl 3-ethylpiperazine-1-carboxylate, a chiral building block widely utilized in chemical synthesis, serves as a crucial precursor in the preparation of various pharmaceutical compounds and organic molecules. This compound plays a significant role in asymmetric synthesis, enabling the creation of enantiomerically pure substances with distinct stereochemical properties. Additionally, its versatile nature allows for the efficient production of complex molecules, making it a valuable tool in medicinal chemistry, materials science, and other research areas. The incorporation of (S)-tert-Butyl 3-ethylpiperazine-1-carboxylate in synthetic routes contributes to the development of novel compounds with enhanced biological activity and targeted functionalities.