142643-29-6 | tert-butyl N-(piperidin-3-ylmethyl)carbamate

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$11.00	$8.00
5g	95%	in stock	$35.00	$25.00
10g	95%	in stock	$68.00	$48.00
25g	95%	in stock	$136.00	$96.00

Description

• Catalog Number: AB63348
• Chemical Name: tert-butyl N-(piperidin-3-ylmethyl)carbamate
• CAS Number: 142643-29-6
• Molecular Formula: C11H22N2O2
• Molecular Weight: 214.3046
• MDL Number: MFCD01632454
• SMILES: O=C(OC(C)(C)C)NCC1CCCNC1

Computed Properties

• Complexity: 211
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 4
• Undefined Atom Stereocenter Count: 1
• XLogP3: 1.2

Upstream Synthesis Route

3-(Boc-aminomethyl)piperidine is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. With its Boc (tert-butyloxycarbonyl) protecting group attached to the amino group, this compound is commonly employed as a building block in organic reactions. The Boc protecting group serves to block the reactivity of the amino group, allowing selective reactions to occur at other functional groups in the molecule.In chemical synthesis, 3-(Boc-aminomethyl)piperidine is often utilized as a key intermediate for the preparation of various bioactive compounds and pharmaceuticals. The presence of the piperidine ring confers important pharmacological properties to the resulting molecules, making this compound particularly valuable in drug discovery research. Furthermore, the Boc protecting group can be easily removed under mild conditions, enabling the selective modification of the amino group to tailor the properties of the final product.Additionally, 3-(Boc-aminomethyl)piperidine can participate in a wide range of transformations such as acylation, alkylation, and cross-coupling reactions, making it a versatile tool in the synthetic chemist's toolbox. Its strategic placement of functional groups allows for efficient and selective derivatization, facilitating the development of complex molecular architectures with high precision. Ultimately, the utility of 3-(Boc-aminomethyl)piperidine in chemical synthesis lies in its ability to serve as a valuable building block for the construction of diverse compounds with tailored properties and functionalities.