301673-16-5 | 4-N-Boc-2-hydroxymethylpiperazine

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$13.00	$9.00
5g	95%	in stock	$25.00	$18.00
10g	95%	in stock	$32.00	$22.00
25g	95%	in stock	$58.00	$40.00

Description

• Catalog Number: AB51213
• Chemical Name: 4-N-Boc-2-hydroxymethylpiperazine
• CAS Number: 301673-16-5
• Molecular Formula: C10H20N2O3
• Molecular Weight: 216.2774
• MDL Number: MFCD04115304
• SMILES: OCC1NCCN(C1)C(=O)OC(C)(C)C

Computed Properties

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

Upstream Synthesis Route

1-Boc-3-hydroxymethylpiperazine, also known as Boc-HMP, is a valuable reagent in chemical synthesis due to its unique properties and versatile applications. As a derivative of piperazine, this compound plays a crucial role in modifying and functionalizing organic molecules. In particular, 1-Boc-3-hydroxymethylpiperazine is commonly used as a protecting group for amines in organic synthesis.By selectively masking the amino group with a Boc (tert-butoxycarbonyl) moiety, 1-Boc-3-hydroxymethylpiperazine facilitates the manipulation of various functional groups within a molecule. This protection strategy enables chemists to differentiate between multiple amine groups in a molecule, allowing for controlled and selective chemical reactions.Moreover, the Boc protecting group can be easily removed under mild conditions, making it a valuable tool in the synthesis of complex organic molecules. The presence of the hydroxymethyl functionality in 1-Boc-3-hydroxymethylpiperazine further expands its utility, offering opportunities for further derivatization and functionalization of target compounds.Overall, 1-Boc-3-hydroxymethylpiperazine is a versatile reagent that finds widespread application in chemical synthesis, particularly in the construction of pharmaceuticals, agrochemicals, and advanced materials. Its ability to selectively protect and manipulate amine groups makes it an indispensable tool for synthetic chemists seeking to design and synthesize novel compounds with tailored properties and functionalities.