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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)-

benzyl (3R)-3-[(1R)-1-amino-3-ethoxy-3-oxopropyl]piperidine-1-carboxylate

CCOC(=O)CC(C1CCCN(C1)C(=O)OCc1ccccc1)N Request for Quotation
Chemical Name: benzyl (3R)-3-[(1R)-1-amino-3-ethoxy-3-oxopropyl]piperidine-1-carboxylate
CAS Number: 886362-35-2
Product Number: AG004A59(AGN-PC-051LQM)
Synonyms:
MDL No:
Molecular Formula: C18H26N2O4
Molecular Weight: 334.4100

Identification/Properties

Properties
BP:
472.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzyl 3-(1-amino-3-ethoxy-3-oxopropyl)piperidine-1-carboxylate is a versatile compound frequently utilized in chemical synthesis due to its significant role as a key intermediate in the production of various pharmaceuticals, fine chemicals, and research molecules. This compound serves as a crucial building block in the creation of complex organic molecules by participating in different chemical transformations, such as amidation, esterification, and ring-closing reactions. Its unique molecular structure imparts specific functional groups that can be selectively modified or manipulated to achieve desired synthetic pathways and target molecules. Additionally, Benzyl 3-(1-amino-3-ethoxy-3-oxopropyl)piperidine-1-carboxylate exhibits stability under various reaction conditions, making it a valuable asset in the synthesis of bioactive compounds and compounds of interest in medicinal chemistry and drug discovery.