144222-22-0 | 1-N-Boc-4-(Aminomethyl)piperidine

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$10.00	$7.00
5g	97%	in stock	$16.00	$11.00
10g	97%	in stock	$25.00	$17.00
25g	97%	in stock	$38.00	$27.00
50g	97%	in stock	$60.00	$42.00
100g	97%	in stock	$119.00	$83.00

Description

• Catalog Number: AB57978
• Chemical Name: 1-N-Boc-4-(Aminomethyl)piperidine
• CAS Number: 144222-22-0
• Molecular Formula: C11H22N2O2
• Molecular Weight: 214.3046
• MDL Number: MFCD01076207
• SMILES: NCC1CCN(CC1)C(=O)OC(C)(C)C

Computed Properties

• Complexity: 215
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 0.9

Upstream Synthesis Route

1-Boc-4-(aminomethyl)piperidine is a versatile compound widely used in chemical synthesis as a valuable building block for the preparation of various pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, characterized by the presence of a Boc-protected amine and an aminomethyl group on a piperidine ring, makes it particularly useful in organic chemistry.One of the key applications of 1-Boc-4-(aminomethyl)piperidine is in the synthesis of complex molecules, where it serves as a key intermediate in the construction of biologically active compounds. By selectively deprotecting the Boc group or modifying the aminomethyl functionality, chemists can efficiently introduce diverse functional groups and stereochemical elements into the target molecules, enabling the creation of new drugs or materials with enhanced properties.Moreover, the presence of the piperidine ring in 1-Boc-4-(aminomethyl)piperidine offers additional synthetic opportunities, as this structural motif is commonly found in many bioactive natural products and pharmaceuticals. By leveraging the chemical reactivity of the piperidine ring, researchers can access a wide range of molecular scaffolds and manipulate their properties to achieve specific biological or physicochemical effects.Overall, 1-Boc-4-(aminomethyl)piperidine plays a crucial role in modern organic synthesis by providing chemists with a strategic tool for building complex molecular architectures and accessing novel chemical space for the development of innovative compounds with potential applications in medicine, agriculture, and materials science.