Di-tert-butyl iminodicarboxylate
98%
- Product Code: 56707
CAS:
51779-32-9
| Molecular Weight: | 217.26 g./mol | Molecular Formula: | C₁₀H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00043309 | |
| Melting Point: | 114-117 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8℃ |
Product Description:
Di-tert-butyl iminodicarboxylate is widely used in organic synthesis as a protecting group for amines. It helps in temporarily masking amine functionalities during multi-step reactions, preventing unwanted side reactions. This compound is particularly valuable in peptide synthesis, where selective protection of amino groups is essential. Additionally, it serves as a key intermediate in the preparation of pharmaceuticals and agrochemicals, enabling the controlled introduction of nitrogen-containing functional groups. Its stability and ease of removal under mild conditions make it a preferred choice in complex synthetic pathways.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97.5 100% |
| APPEARANCE | White to Faint Yellow Powder or Crystals |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿340.00 |
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| 5.000 | 10-20 days | ฿530.00 |
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| 25.000 | 10-20 days | ฿1,880.00 |
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| 100.000 | 10-20 days | ฿6,980.00 |
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Di-tert-butyl iminodicarboxylate
Di-tert-butyl iminodicarboxylate is widely used in organic synthesis as a protecting group for amines. It helps in temporarily masking amine functionalities during multi-step reactions, preventing unwanted side reactions. This compound is particularly valuable in peptide synthesis, where selective protection of amino groups is essential. Additionally, it serves as a key intermediate in the preparation of pharmaceuticals and agrochemicals, enabling the controlled introduction of nitrogen-containing functional groups. Its stability and ease of removal under mild conditions make it a preferred choice in complex synthetic pathways.
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