1. Home
  2. (S)-1-Boc-4-benzyl-2-(hydroxymethyl)piperazine

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

(S)-1-Boc-4-benzyl-2-(hydroxymethyl)piperazine

OC[C@@H]1CN(CCN1C(=O)OC(C)(C)C)Cc1ccccc1 Request for Quotation
Chemical Name: (S)-1-Boc-4-benzyl-2-(hydroxymethyl)piperazine
CAS Number: 947275-34-5
Product Number: AG005VQ0(AGN-PC-0ONY2L)
Synonyms:
MDL No:
Molecular Formula: C17H26N2O3
Molecular Weight: 306.3999

Identification/Properties

Properties
Storage:
2-8℃;Keep in dry area;
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


(S)-1-Boc-4-benzyl-2-(hydroxymethyl)piperazine is a valuable compound commonly used in chemical synthesis as a chiral building block. Its unique structure, featuring a Boc (tert-butoxycarbonyl) protecting group and a benzyl group attached to a piperazine ring with a hydroxymethyl functional group, offers versatility in various synthetic routes.This compound plays a crucial role in the preparation of pharmaceutical intermediates and bioactive molecules due to its chiral nature. The Boc protecting group can be selectively removed under mild conditions, allowing for further functionalization of the piperazine core. The benzyl group provides stability during various reaction conditions while the hydroxymethyl group serves as a reactive site for further derivatization.In chemical synthesis, (S)-1-Boc-4-benzyl-2-(hydroxymethyl)piperazine is often utilized in asymmetric synthesis to introduce chirality into molecules, which is essential for the development of enantiopure compounds with specific biological activities. Its presence enables the creation of complex molecules with high stereochemical control, making it a versatile tool for organic chemists in the design and synthesis of new compounds for pharmaceutical and medicinal applications.