169448-87-7 | tert-butyl (2R)-2-(hydroxymethyl)piperazine-1-carboxylate

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$10.00	$7.00
250mg	95%	in stock	$13.00	$10.00
1g	95%	in stock	$28.00	$19.00
5g	95%	in stock	$99.00	$69.00
10g	95%	in stock	$196.00	$137.00

Description

• Catalog Number: AB42881
• Chemical Name: tert-butyl (2R)-2-(hydroxymethyl)piperazine-1-carboxylate
• CAS Number: 169448-87-7
• Molecular Formula: C10H20N2O3
• Molecular Weight: 216.2774
• MDL Number: MFCD07772092
• SMILES: OC[C@H]1CNCCN1C(=O)OC(C)(C)C

Computed Properties

• Complexity: 225
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• XLogP3: -0.2

Upstream Synthesis Route

(R)-1-Boc-2-(Hydroxymethyl)piperazine is a versatile compound commonly utilized in chemical synthesis for its unique reactivity and functional groups. This compound serves as a valuable building block in organic synthesis due to its chiral nature and potential for selective transformations. Specifically, it is commonly employed as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals.One prominent application of (R)-1-Boc-2-(Hydroxymethyl)piperazine is in the synthesis of chiral compounds, where its chiral center imparts stereochemical control on the reaction outcome. By utilizing this compound as a starting material, chemists can access enantiomerically pure products, crucial in the pharmaceutical industry where chirality often dictates biological activity.Additionally, the hydroxymethyl group on the piperazine ring offers a reactive handle for further functionalization through various chemical reactions such as acylation, alkylation, and oxidation. This allows for the introduction of diverse functional groups, expanding the chemical versatility and synthetic potential of (R)-1-Boc-2-(Hydroxymethyl)piperazine in complex molecule construction.