169447-70-5 | (S)-1-N-Boc-2-methylpiperazine

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$8.00	$5.00
5g	95%	in stock	$14.00	$10.00
10g	95%	in stock	$25.00	$18.00
25g	95%	in stock	$59.00	$41.00
50g	95%	in stock	$103.00	$72.00

Description

• Catalog Number: AB42956
• Chemical Name: (S)-1-N-Boc-2-methylpiperazine
• CAS Number: 169447-70-5
• Molecular Formula: C10H20N2O2
• Molecular Weight: 200.278
• MDL Number: MFCD01862121
• SMILES: C[C@H]1CNCCN1C(=O)OC(C)(C)C

Computed Properties

• Complexity: 211
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 0.9

Upstream Synthesis Route

(S)-1-N-Boc-2-methylpiperazine, also known as (S)-N-tert-butoxycarbonyl-2-methylpiperazine, is a valuable chiral building block commonly used in chemical synthesis for the asymmetric preparation of pharmaceuticals, agrochemicals, and other fine chemicals. This compound plays a crucial role in the synthesis of various biologically active molecules due to its chirality and robust chemical reactivity.One of the prominent applications of (S)-1-N-Boc-2-methylpiperazine is in the development of chiral ligands for asymmetric catalysis. By incorporating this compound into the structure of ligands, chemists can efficiently control the stereochemistry of their target molecules, enabling the selective formation of enantiomerically pure products. This capability is particularly significant in the pharmaceutical industry, where the activity and safety of drugs often depend on the specific arrangement of functional groups in the molecule.Additionally, (S)-1-N-Boc-2-methylpiperazine serves as a key intermediate in the synthesis of various pharmaceutical agents, such as chiral amines, amino alcohols, and heterocyclic compounds. Its versatile chemistry allows for the introduction of diverse functional groups and structural motifs, facilitating the creation of complex molecular architectures with high levels of stereocontrol. This compound's role in chemical synthesis highlights its importance as a crucial building block in the production of chirally pure compounds with diverse applications in the field of medicinal chemistry and beyond.