(S)-tert-Butyl 2-benzylpiperazine-1-carboxylate, CAS No. 169447-86-3

Welcome to iChemical.com!

In the below part, please select the country you want us to ship to: Please note that once you've selected a shipping country, all pricing information on our website will be automatically updated to include door-to-door shipping to the country you specified.

North America

South America

Africa

Europe

Asia

Oceania

169447-86-3

Catalog No. EBD2210390

CAS 169447-86-3

Name (S)-tert-Butyl 2-benzylpiperazine-1-carboxylate

Get Quote

Basic Information

Synonyms: (S)-tert-Butyl2-benzylpiperazine-1-carboxylate 2s-benzyl-piperazine-1-carboxylicacidtert-butylester (s)-n1-boc-2-benzylpiperazine (s)-2-benzyl-piperazine-1-carboxylicacidtert-butylester (s)-1-n-boc-2-benzyl-piperazine (s)-1-boc-2-benzyl-piperazine (s)-1-boc-2-benzylpiperizine (s)-1-boc-2-benzyl-piperazine98% (s)-2-benzylpiperazine,n1-bocprotected (s)-1-boc-2-benzylpiperazine tert-butyl(2S)-2-benzylpiperazine-1-carboxylate

Molecular Formula: C16H24N2O2

Molecular Weight: 276.37

MDL Number: MFCD03787923

Categories: Medicinal Chemistry > Pharmaceutical Intermediates > Heterocyclic Intermediates Synthetic Chemistry > Organic Building Blocks > Amines

Product Description:

(S)-1-Boc-2-Benzylpiperazine is a chiral piperazine derivative characterized by a tert-butoxycarbonyl (Boc) protecting group on one nitrogen and a benzyl group on the other. This specific stereochemistry (S-configuration) is crucial for its application in asymmetric synthesis. Its primary and most significant application is as a key chiral building block in pharmaceutical research and development. It serves as a versatile intermediate for the synthesis of various bioactive molecules, particularly in constructing complex heterocyclic scaffolds found in drug candidates. The Boc group provides orthogonal protection, allowing for selective deprotection and further functionalization, which is essential in multi-step synthetic routes. While its main utility is in medicinal chemistry as a specialized intermediate, its well-defined structure and functional groups also make it a valuable reagent in general organic synthesis for constructing chiral amine-containing compounds.

Physical Properties