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Home  > (3S)-1,3-Dimethylpiperazine

AA21169

1152367-80-0 | (3S)-1,3-Dimethylpiperazine

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $33.00 $23.00 -   +
250mg 95% in stock $52.00 $37.00 -   +
1g 95% in stock $68.00 $48.00 -   +
2500mg 95% in stock $120.00 $84.00 -   +
5g 95% in stock $232.00 $162.00 -   +
25g 95% in stock $822.00 $576.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA21169
Chemical Name: (3S)-1,3-Dimethylpiperazine
CAS Number: 1152367-80-0
Molecular Formula: C6H14N2
Molecular Weight: 114.1888
MDL Number: MFCD11114436
SMILES: CN1CCN[C@H](C1)C

 

Upstream Synthesis Route
  • (3S)-1,3-Dimethylpiperazine, a chiral compound, plays a key role in various chemical synthesis processes. Its unique structure consisting of a piperazine ring with two methyl groups attached at the 1 and 3 positions offers diverse opportunities for selective reactions and building complex molecular frameworks.In organic synthesis, (3S)-1,3-Dimethylpiperazine is commonly utilized as a chiral building block to introduce asymmetry into molecules. Its chirality facilitates the creation of enantiopure compounds, which are highly valuable in pharmaceutical, agrochemical, and material science industries. The presence of a piperazine ring in its structure also imparts distinctive properties that can be exploited in the design of bioactive molecules and coordination complexes.Furthermore, (3S)-1,3-Dimethylpiperazine serves as a versatile ligand in coordination chemistry, forming stable complexes with transition metal ions. These complexes can act as catalysts in a wide range of organic transformations, including asymmetric hydrogenation, cross-coupling reactions, and cycloadditions. The unique steric and electronic properties of (3S)-1,3-Dimethylpiperazine contribute to the selectivity and efficiency of these catalytic processes.Overall, (3S)-1,3-Dimethylpiperazine is a valuable building block with diverse applications in chemical synthesis, providing chemists with powerful tools for the construction of intricate molecular architectures and the development of innovative synthetic methodologies.
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