(R)-3-AMINO-PIPERIDINE-1-CARBOXYLIC ACID BENZYL ESTER HYDROCHLORIDE|1217781-62-8,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

(R)-3-AMINO-PIPERIDINE-1-CARBOXYLIC ACID BENZYL ESTER HYDROCHLORIDE

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Chemical Name:	(R)-3-AMINO-PIPERIDINE-1-CARBOXYLIC ACID BENZYL ESTER HYDROCHLORIDE
CAS Number:	1217781-62-8
Product Number:	AG0015Y5(AGN-PC-0WAKKH)
Synonyms:
MDL No:
Molecular Formula:	C13H19ClN2O2
Molecular Weight:	270.7552

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Identification/Properties

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Keep in dry area;Room Temperature;

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Chemical Structure

(R)-Benzyl 3-aminopiperidine-1-carboxylate hydrochloride is a valuable compound widely utilized in chemical synthesis due to its versatile reactivity and functional group capabilities. This compound serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its chirality, resulting from the (R)-configuration, plays a crucial role in determining the stereochemistry of the final products, making it highly important in asymmetric synthesis. By incorporating (R)-Benzyl 3-aminopiperidine-1-carboxylate hydrochloride into synthetic routes, chemists can efficiently access a range of enantiopure molecules with enhanced biological activities or desired properties. Additionally, this compound's stability and compatibility with different reaction conditions further enhance its utility in producing complex molecules with high purity and yield. In summary, (R)-Benzyl 3-aminopiperidine-1-carboxylate hydrochloride is a strategic building block that enables access to diverse chemical structures and is instrumental in advancing the field of chemical synthesis.