Ethyl 2-(1-Boc-4-piperidylidene)acetate

≥95%

  • Product Code: 58255
  CAS:    135716-08-4
Molecular Weight: 269.34 g./mol Molecular Formula: C₁₄H₂₃NO₄
EC Number: MDL Number: MFCD12912655
Melting Point: Boiling Point:
Density: Storage Condition: room temperature, dry
Product Description: Ethyl 2-(1-Boc-4-piperidylidene)acetate is widely used in organic synthesis as a versatile intermediate. It plays a key role in the preparation of pharmaceuticals, particularly in the development of compounds with potential therapeutic effects. Its structure is valuable for constructing complex molecules, especially those involving piperidine scaffolds, which are common in drug discovery. The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions, making it useful in multi-step synthetic processes. Additionally, it is employed in the synthesis of biologically active compounds, including those targeting neurological disorders and other medical conditions. Its ester functionality also makes it suitable for further modifications, enhancing its utility in medicinal chemistry.
Product Specification:
Test Specification
APPEARANCE White to Very pale yellow Crystal or Powder
PURITY 95-100
MELTING POINT 83.0-87.0
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $59.39
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5.000 10-20 days $179.82
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25.000 10-20 days $638.72
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Ethyl 2-(1-Boc-4-piperidylidene)acetate
Ethyl 2-(1-Boc-4-piperidylidene)acetate is widely used in organic synthesis as a versatile intermediate. It plays a key role in the preparation of pharmaceuticals, particularly in the development of compounds with potential therapeutic effects. Its structure is valuable for constructing complex molecules, especially those involving piperidine scaffolds, which are common in drug discovery. The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions, making it useful in multi-step synthetic processes. Additionally, it is employed in the synthesis of biologically active compounds, including those targeting neurological disorders and other medical conditions. Its ester functionality also makes it suitable for further modifications, enhancing its utility in medicinal chemistry.
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