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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-Piperidinecarboxylic acid, 4-(3-hydroxypropyl)-, phenylmethyl ester

OCCCC1CCN(CC1)C(=O)OCc1ccccc1 Request for Quotation
Chemical Name: 1-Piperidinecarboxylic acid, 4-(3-hydroxypropyl)-, phenylmethyl ester
CAS Number: 99198-80-8
Product Number: AG006PDB(AGN-PC-0038GL)
Synonyms:
MDL No:
Molecular Formula: C16H23NO3
Molecular Weight: 277.3587

Identification/Properties

Properties
Form:
Solid

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
N/A
Hazard Statements:
-
Precautionary Statements:
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


This compound, 4-(3-hydroxypropyl)-piperidine-1-carboxylic acid benzyl ester, is a versatile intermediate commonly used in chemical synthesis. Its unique molecular structure allows for a range of applications in organic chemistry, particularly in the production of pharmaceuticals and fine chemicals.One of the key applications of this compound is its use as a building block in the synthesis of bioactive molecules. The presence of the piperidine ring and the benzyl ester group enables the compound to participate in various chemical reactions, such as acylation, alkylation, and cyclization. These reactions can be further manipulated to introduce additional functional groups onto the molecule, thereby expanding its potential for diverse chemical transformations.Moreover, the hydroxypropyl group attached to the piperidine ring provides a site for further derivatization, allowing for the modification of the compound's chemical properties and reactivity. This versatility makes 4-(3-hydroxypropyl)-piperidine-1-carboxylic acid benzyl ester a valuable precursor in the synthesis of complex molecules with specific biological activities or physical properties.Overall, the strategic positioning of functional groups within this compound makes it a valuable tool for organic chemists seeking to design and construct novel compounds for various applications in the field of drug discovery, materials science, and chemical biology.