tert-Butyl (R)-2-Methylpiperazine-1-carboxylate TCI B6400

Chemical Identity

Other names: (R)-1-Boc-2-methylpiperazine · (R)-N-(tert-Butoxycarbonyl)-2-methylpiperazine · (R)-2-Methylpiperazine-1-carboxylic Acid tert-Butyl Ester
CAS No.: 170033-47-3
PubChem: CID 10262201
Formula: C10H20N2O2
Molecular weight: 200.28 g/mol
Purity: >98.0%(GC)
Storage: 0-10°C
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: tert-butyl (2R)-2-methylpiperazine-1-carboxylate
SMILES: CC1CNCCN1C(=O)OC(C)(C)C
InChIKey: DATRVIMZZZVHMP-MRVPVSSYSA-N
MDL: MDL01862120

Rp 1.113.000,00

~~Rp 793.800,00~~ Rp 1.113.000,00

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Berat 1g 5g

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TCI B6400, tert-butyl (R)-2-methylpiperazine-1-carboxylate (CAS 170033-47-3), is a mono-Boc-protected chiral piperazine building block with defined (R) configuration at C-2. The selective protection leaves the N-4 nitrogen free for alkylation, acylation, sulfonylation, reductive amination, or Buchwald–Hartwig coupling. Subsequent acid-mediated Boc removal unmasks the second nitrogen for further elaboration, making the reagent well suited to multi-step medicinal chemistry routes. AMI Scientific supplies it in 1 g and 5 g packs; refer to the lot Certificate of Analysis for stereochemical and purity data.

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STUDER et al. (1995). ChemInform Abstract: Synthesis and First Applications of a New Chiral Auxiliary (tert‐Butyl 2‐(tert‐Butyl)‐5,5‐dimethyl‐4‐oxoimidazolidine‐1‐carboxylate) (V).. ChemInform doi:10.1002/chin.199547157
Mamat et al. (2012). Synthesis and Molecular Structure of tert-Butyl 4-(2-tert-butoxy-2-oxoethyl)piperazine-1-carboxylate. Crystals doi:10.3390/cryst2010090
Grauer et al. (2009). Synthesis of rac-tert-butyl 3-(benzyloxycarbonylamino)-2-(4-bromophenyl)-tetrahydrofuran-3-carboxylate. Molbank doi:10.3390/m596

References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.