Ethyl 2-(1-Boc-4-piperidylidene)acetate
≥95%
- Product Code: 58255
CAS:
135716-08-4
Molecular Weight: | 269.34 g./mol | Molecular Formula: | C₁₄H₂₃NO₄ |
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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 |
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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 |
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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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