Cas no 867009-56-1 (1-tert-Butyl 4-ethyl 4-(2-ethoxy-2-oxoethyl)-piperidine-1,4-dicarboxylate)

1-tert-Butyl 4-ethyl 4-(2-ethoxy-2-oxoethyl)-piperidine-1,4-dicarboxylate is a versatile intermediate in organic synthesis, particularly valuable for the construction of functionalized piperidine derivatives. Its structure features both tert-butyl and ethyl ester groups, offering selective reactivity for further modifications. The 2-ethoxy-2-oxoethyl substituent enhances its utility in nucleophilic and electrophilic transformations, making it a useful precursor for pharmaceuticals and agrochemicals. The compound’s stability under standard conditions ensures ease of handling and storage. Its well-defined stereochemistry and high purity make it suitable for applications requiring precise molecular control, such as medicinal chemistry and materials science. This intermediate is particularly advantageous for multistep synthetic routes due to its orthogonal protecting groups.
1-tert-Butyl 4-ethyl 4-(2-ethoxy-2-oxoethyl)-piperidine-1,4-dicarboxylate structure
867009-56-1 structure
Product Name:1-tert-Butyl 4-ethyl 4-(2-ethoxy-2-oxoethyl)-piperidine-1,4-dicarboxylate
CAS No:867009-56-1
MF:C17H29NO6
MW:343.415265798569
CID:844387
PubChem ID:52987806
Update Time:2025-05-22

1-tert-Butyl 4-ethyl 4-(2-ethoxy-2-oxoethyl)-piperidine-1,4-dicarboxylate Chemical and Physical Properties

Names and Identifiers

    • 1-tert-Butyl 4-ethyl 4-(2-ethoxy-2-oxoethyl)piperidine-1,4-dicarboxylate
    • 1,4-Piperidinedicarboxylic acid, 4-(2-ethoxy-2-oxoethyl)-, 1-(1,1-dimethylethyl) 4-ethyl ester
    • 1-tert-Butyl 4-ethyl 4-(2-ethoxy-2-oxoethyl)-piperidine-1,4-dicarboxylate
    • 4-(2-Ethoxy-2-oxoethyl)-1,4-piperidine dicarboxylic acid 1-(1,1-dimethylethyl) 4-ethyl ester
    • 1-(Tert-butyl) 4-ethyl 4-(2-ethoxy-2-oxoethyl)piperidine-1,4-dicarboxylate
    • DTXSID601133220
    • CS-0456669
    • 1-O-tert-butyl 4-O-ethyl 4-(2-ethoxy-2-oxoethyl)piperidine-1,4-dicarboxylate
    • FT-0727503
    • 1-tert-Butyl4-ethyl4-(2-ethoxy-2-oxoethyl)piperidine-1,4-dicarboxylate
    • 867009-56-1
    • 1-(1,1-Dimethylethyl) 4-ethyl 4-(2-ethoxy-2-oxoethyl)-1,4-piperidinedicarboxylate
    • MDL： MFCD17215372
    • Inchi： 1S/C17H29NO6/c1-6-22-13(19)12-17(14(20)23-7-2)8-10-18(11-9-17)15(21)24-16(3,4)5/h6-12H2,1-5H3
    • InChI Key： SXZLSDSEEKQYPA-UHFFFAOYSA-N
    • SMILES： O(CC)C(C1(CC(=O)OCC)CCN(C(=O)OC(C)(C)C)CC1)=O

Computed Properties

  • Exact Mass: 343.19948764g/mol
  • Monoisotopic Mass: 343.19948764g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 7
  • Heavy Atom Count: 24
  • Rotatable Bond Count: 10
  • Complexity: 460
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.8
  • Topological Polar Surface Area: 82.1?2

1-tert-Butyl 4-ethyl 4-(2-ethoxy-2-oxoethyl)-piperidine-1,4-dicarboxylate Pricemore >>

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1-tert-Butyl 4-ethyl 4-(2-ethoxy-2-oxoethyl)-piperidine-1,4-dicarboxylate Related Literature

Additional information on 1-tert-Butyl 4-ethyl 4-(2-ethoxy-2-oxoethyl)-piperidine-1,4-dicarboxylate

Comprehensive Overview of 1-tert-Butyl 4-ethyl 4-(2-ethoxy-2-oxoethyl)-piperidine-1,4-dicarboxylate (CAS No. 867009-56-1)

1-tert-Butyl 4-ethyl 4-(2-ethoxy-2-oxoethyl)-piperidine-1,4-dicarboxylate (CAS No. 867009-56-1) is a highly specialized organic compound with significant applications in pharmaceutical and chemical research. This compound belongs to the class of piperidine derivatives, which are widely recognized for their role in drug discovery and development. The unique structural features of this molecule, including the tert-butyl and ethyl ester groups, make it a valuable intermediate in the synthesis of bioactive molecules.

In recent years, the demand for piperidine-based compounds has surged due to their versatility in medicinal chemistry. Researchers are particularly interested in CAS No. 867009-56-1 for its potential as a building block in the development of central nervous system (CNS) therapeutics. The compound's dicarboxylate functionality allows for further chemical modifications, enabling the creation of novel drug candidates. This aligns with the growing trend of precision medicine and targeted drug delivery, which are hot topics in the pharmaceutical industry.

The synthesis of 1-tert-Butyl 4-ethyl 4-(2-ethoxy-2-oxoethyl)-piperidine-1,4-dicarboxylate involves multi-step organic reactions, including esterification and alkylation processes. These methods are well-documented in peer-reviewed journals, making this compound accessible to researchers worldwide. Its high purity and stability under standard laboratory conditions further enhance its appeal as a research chemical. The compound's molecular weight and solubility properties are also critical factors for its use in various experimental setups.

From an industrial perspective, CAS No. 867009-56-1 is often discussed in the context of green chemistry and sustainable synthesis. Companies are increasingly focusing on eco-friendly production methods, and this compound's synthesis can be optimized to minimize waste and energy consumption. This aligns with the global push toward environmentally responsible manufacturing, a topic frequently searched by professionals in the chemical sector.

Another area of interest is the compound's potential role in peptide mimetics and enzyme inhibitors. The piperidine core of 1-tert-Butyl 4-ethyl 4-(2-ethoxy-2-oxoethyl)-piperidine-1,4-dicarboxylate is structurally similar to many natural alkaloids, making it a candidate for the development of bioactive scaffolds. This has led to increased searches for piperidine derivatives in drug design, as researchers explore new ways to combat diseases like cancer and neurodegenerative disorders.

In summary, 1-tert-Butyl 4-ethyl 4-(2-ethoxy-2-oxoethyl)-piperidine-1,4-dicarboxylate (CAS No. 867009-56-1) is a compound of significant scientific and industrial relevance. Its applications span from pharmaceutical intermediates to green chemistry initiatives, making it a subject of ongoing research and development. As the demand for innovative chemical solutions grows, this compound is poised to play a pivotal role in advancing both academic and industrial projects.

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