848482-93-9 | (S)-4-BOC-Piperazine-2-carboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$13.00	$9.00
1g	97%	in stock	$30.00	$21.00
5g	97%	in stock	$65.00	$45.00
10g	97%	in stock	$124.00	$87.00
25g	97%	in stock	$301.00	$211.00

Description

• Catalog Number: AB50651
• Chemical Name: (S)-4-BOC-Piperazine-2-carboxylic acid
• CAS Number: 848482-93-9
• Molecular Formula: C10H18N2O4
• Molecular Weight: 230.2609
• MDL Number: MFCD02179098
• SMILES: OC(=O)[C@H]1NCCN(C1)C(=O)OC(C)(C)C

Computed Properties

• Complexity: 285
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• XLogP3: -2.2

Upstream Synthesis Route

(S)-1-N-Boc-piperazine-3-carboxylic acid is a valuable intermediate in chemical synthesis, particularly in the pharmaceutical industry. This compound serves as a key building block for the preparation of various biologically active molecules and pharmaceuticals. Its chiral nature, derived from the presence of the Boc (tert-butoxycarbonyl) protecting group and the piperazine ring, makes it a versatile tool in asymmetric synthesis.One notable application of (S)-1-N-Boc-piperazine-3-carboxylic acid is in the synthesis of potential drug candidates targeting the central nervous system. By utilizing the chiral properties of this compound, chemists can access enantiomerically pure derivatives that exhibit enhanced biological activity and selectivity, crucial for drug development.Additionally, (S)-1-N-Boc-piperazine-3-carboxylic acid can be employed in the construction of complex organic molecules through various transformations such as amide bond formation, cyclization reactions, and substitution reactions. Its presence in the synthetic toolbox allows for the efficient and selective incorporation of the piperazine motif into diverse chemical structures, enabling the exploration of novel drug candidates and biologically active compounds.