(R)-Benzyl 3-(hydroxymethyl)piperazine-1-carboxylate hydrochloride|930782-91-5,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)-Benzyl 3-(hydroxymethyl)piperazine-1-carboxylate hydrochloride

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Chemical Name:	(R)-Benzyl 3-(hydroxymethyl)piperazine-1-carboxylate hydrochloride
CAS Number:	930782-91-5
Product Number:	AG006J3L(AGN-PC-0WAHSL)
Synonyms:
MDL No:
Molecular Formula:	C13H19ClN2O3
Molecular Weight:	286.7546

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Identification/Properties

Properties

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Keep in dry area;Room Temperature;

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Chemical Structure

(R)-Benzyl 3-(hydroxymethyl)piperazine-1-carboxylate hydrochloride is a versatile compound commonly utilized in chemical synthesis as a chiral building block. Its unique structure offers a valuable tool for the preparation of various pharmaceutical intermediates and fine chemicals. Due to the presence of a piperazine ring and a hydroxymethyl group, this compound serves as a key component in the synthesis of complex molecules with desirable chirality and biological activities. Its application in asymmetric synthesis and drug development makes it an essential reagent for the production of enantiomerically pure compounds with potential pharmacological properties.