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AB42978

216854-23-8 | (S)-3-Boc-aminopiperidine

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $8.00 $5.00 -   +
5g 98% in stock $10.00 $7.00 -   +
10g 98% in stock $15.00 $10.00 -   +
25g 98% in stock $25.00 $17.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB42978
Chemical Name: (S)-3-Boc-aminopiperidine
CAS Number: 216854-23-8
Molecular Formula: C10H20N2O2
Molecular Weight: 200.27800000000005
MDL Number: MFCD03093383
SMILES: O=C(OC(C)(C)C)N[C@H]1CCCNC1

 

Computed Properties
Complexity: 199  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 3  
XLogP3: 1.1  

 

 

Upstream Synthesis Route
  • (S)-3-N-Boc-Aminopiperidine is a valuable building block in chemical synthesis due to its versatile applications in the production of pharmaceuticals, agrochemicals, and materials. With its unique structure and reactivity, this compound serves as a propitious intermediate in the synthesis of various complex molecules.One of the primary uses of (S)-3-N-Boc-Aminopiperidine is in the preparation of chiral compounds. Its chirality confers distinct stereochemical properties to the molecules synthesized from it, making it crucial in the production of enantiomerically pure substances. This is particularly important in the pharmaceutical industry, where the efficacy and safety of drugs often depend on the specific arrangement of atoms in the molecule.Additionally, (S)-3-N-Boc-Aminopiperidine can be utilized in the construction of heterocyclic compounds. Its incorporation into rings can lead to the formation of diverse structures with unique electronic and steric properties. These heterocycles find applications in a wide range of fields, including medicinal chemistry and materials science.Furthermore, the presence of the Boc protecting group on the amino group of 3-N-Boc-Aminopiperidine provides an extra level of control in chemical transformations. The Boc group can be selectively removed under mild conditions, allowing for further functionalization of the amine moiety. This feature enhances the synthetic versatility of (S)-3-N-Boc-Aminopiperidine, enabling the synthesis of a myriad of compounds with tailored properties.In conclusion, (S)-3-N-Boc-Aminopiperidine plays a pivotal role in chemical synthesis by serving as a fundamental building block for the construction of complex molecules with specific stereochemical and functional properties. Its utility in synthesizing chiral compounds, heterocycles, and protected amines makes it an indispensable tool for researchers and chemists working across various disciplines.
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