879275-33-9 | (R)-3-(Boc-aminomethyl)piperidine

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$25.00	$17.00
5g	95%	in stock	$69.00	$48.00
10g	95%	in stock	$89.00	$63.00
25g	95%	in stock	$196.00	$137.00
50g	95%	in stock	$352.00	$247.00
100g	95%	in stock	$602.00	$421.00

Description

• Catalog Number: AH91244
• Chemical Name: (R)-3-(Boc-aminomethyl)piperidine
• CAS Number: 879275-33-9
• Molecular Formula: C11H22N2O2
• Molecular Weight: 214.3046
• MDL Number: MFCD03093384
• SMILES: O=C(OC(C)(C)C)NC[C@@H]1CCCNC1

Computed Properties

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

Upstream Synthesis Route

The (R)-tert-Butyl (piperidin-3-ylmethyl)carbamate, also known as $name$, serves as a valuable reagent in chemical synthesis due to its unique properties. This compound is widely utilized as a chiral building block in asymmetric synthesis, allowing for the introduction of chirality in various target molecules.$name$ is frequently employed in the synthesis of pharmaceutical compounds, agrochemicals, and fine chemicals where stereochemical control is crucial. Its chiral nature enables the formation of enantiomerically pure products, making it an essential tool in the production of optically active compounds.In addition, $name$ can act as a protective group for amines, safeguarding their reactivity during specific synthetic transformations. This property enhances the selectivity of reactions and facilitates the synthesis of complex organic molecules.Furthermore, the presence of the tert-butyl and piperidine motifs in $name$ imparts steric hindrance and enhanced stability to the molecule, making it suitable for diverse chemical reactions. Its compatibility with a variety of functional groups makes it a versatile building block in organic chemistry.Overall, the application of (R)-tert-Butyl (piperidin-3-ylmethyl)carbamate in chemical synthesis enables chemists to access enantioenriched compounds and streamline the synthesis of complex molecules with precise stereochemical control.