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Home  > Chemistry  > Heterocyclic Building Blocks  > Piperidines  > 3,3-Dimethylglutarimide

AB66267

1123-40-6 | 3,3-Dimethylglutarimide

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $10.00 $7.00 -   +
5g 98% in stock $28.00 $19.00 -   +
10g 98% in stock $35.00 $24.00 -   +
25g 98% in stock $80.00 $56.00 -   +
100g 98% in stock $286.00 $200.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB66267
Chemical Name: 3,3-Dimethylglutarimide
CAS Number: 1123-40-6
Molecular Formula: C7H11NO2
Molecular Weight: 141.1677
MDL Number: MFCD00006671
SMILES: O=C1NC(=O)CC(C1)(C)C

 

Computed Properties
Complexity: 166  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
XLogP3: 0.2  

 

 

Upstream Synthesis Route
  • 4,4-Dimethylpiperidine-2,6-dione is a versatile organic compound widely utilized in chemical synthesis processes. Its unique structure and reactivity make it a valuable building block for the creation of various complex molecules in the field of organic chemistry. In particular, this compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals.One notable application of 4,4-Dimethylpiperidine-2,6-dione is its role as a precursor in the synthesis of heterocyclic compounds, which are essential in drug discovery and development. By incorporating this compound into reactions, chemists can access a diverse range of heterocyclic structures that exhibit valuable biological activities. Additionally, 4,4-Dimethylpiperidine-2,6-dione can participate in various cyclization reactions to form ring structures, enabling the construction of complex molecular frameworks efficiently.Furthermore, this compound can be used in the preparation of ligands for transition metal-catalyzed reactions, enabling the selective formation of desired products in organic transformations. Its ability to chelate with metal ions enhances catalytic efficiency and facilitates the synthesis of target molecules with high stereochemical control.Overall, 4,4-Dimethylpiperidine-2,6-dione plays a crucial role in the development of novel chemical entities with diverse applications, making it an indispensable tool in the field of chemical synthesis.
Literature
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