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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-(phenylmethoxycarbonylamino)piperidine-1-carboxylate

O=C(NC1CCN(CC1)C(=O)OC(C)(C)C)OCc1ccccc1 Request for Quotation
Chemical Name: tert-butyl 4-(phenylmethoxycarbonylamino)piperidine-1-carboxylate
CAS Number: 220394-97-8
Product Number: AG007Q4Q(AGN-PC-0K6A4K)
Synonyms:
MDL No: MFCD04038520
Molecular Formula: C18H26N2O4
Molecular Weight: 334.4100

Identification/Properties

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


1-Boc-4-(Cbz-amino)piperidine is a versatile compound commonly employed in chemical synthesis as a protecting group strategy. This compound acts as a dual protecting group, with the t-Boc (tert-butyloxycarbonyl) and Cbz (benzyloxycarbonyl) groups shielding the amino and piperidine functionalities, respectively. In organic synthesis, 1-Boc-4-(Cbz-amino)piperidine can be utilized as a key building block in the synthesis of various complex molecules, particularly in the preparation of pharmaceutical intermediates and natural product derivatives. The presence of both protective groups allows for selective deprotection and functional group manipulation at desired stages of the synthesis, ensuring the preservation of the target molecule's stereochemistry and reactivity.Furthermore, the compatibility of 1-Boc-4-(Cbz-amino)piperidine with a wide range of reaction conditions and functional groups makes it a valuable tool in the synthesis of peptide mimetics, drug candidates, and bioactive compounds. This compound's strategic use in chemical synthesis facilitates efficient and precise control over the structural modifications necessary for the development of new molecules with improved pharmacological properties and biological activities.