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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-[2-(phenylmethoxycarbonylamino)ethyl]piperazine-1-carboxylate

O=C(OCc1ccccc1)NCCN1CCN(CC1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 4-[2-(phenylmethoxycarbonylamino)ethyl]piperazine-1-carboxylate
CAS Number: 302557-32-0
Product Number: AG002ZDF(AGN-PC-059B2O)
Synonyms:
MDL No:
Molecular Formula: C19H29N3O4
Molecular Weight: 363.4513

Identification/Properties

Properties
BP:
505.1°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
363.458g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
8
Exact Mass:
363.216g/mol
Monoisotopic Mass:
363.216g/mol
Topological Polar Surface Area:
71.1A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
450
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 4-(2-(((benzyloxy)carbonyl)amino)ethyl)piperazine-1-carboxylate compound is commonly used in chemical synthesis as a versatile building block for creating complex organic molecules. Its structure contains a piperazine ring with an ethyl functional group, as well as a benzyloxy carbonyl protecting group. This compound is particularly useful in the formation of peptide and drug molecules due to its stability and reactivity. In chemical synthesis, tert-Butyl 4-(2-(((benzyloxy)carbonyl)amino)ethyl)piperazine-1-carboxylate can be selectively deprotected, reacted with other molecules, or modified to introduce new functional groups, allowing for the creation of diverse and intricate chemical structures. Its applications extend to the development of pharmaceuticals, agrochemicals, and materials science, providing a valuable tool for synthetic chemists seeking to engineer novel compounds with specific properties and functions.