4-Ethyl-2,3-dioxo-1-piperazine carbonyl chloride
95%
- Product Code: 118818
Alias:
4-Ethyl-2,3-dioxo-1-piperazinecarbonyl chloride (EDPC) ; Dioxypiperazinecarbonyl chloride
CAS:
59703-00-3
| Molecular Weight: | 204.61 g./mol | Molecular Formula: | C₇H₉ClN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00067054 | |
| Melting Point: | 100 °C | Boiling Point: | |
| Density: | Storage Condition: | 2~8℃, dry, sealed |
Product Description:
This compound is primarily utilized in the synthesis of various pharmaceutical intermediates, particularly in the development of antibiotics and other therapeutic agents. Its reactive carbonyl chloride group makes it a valuable building block in organic synthesis, enabling the formation of amide bonds with amines or other nucleophiles. It is often employed in the preparation of piperazine derivatives, which are key structural components in many drugs targeting bacterial infections, central nervous system disorders, and cardiovascular diseases. Additionally, its use in peptide coupling reactions is significant for creating complex molecular structures in medicinal chemistry. The compound's versatility and reactivity make it a crucial reagent in the production of biologically active molecules.
Product Specification:
| Test | Specification |
|---|---|
| Absorption (400 Nm) | 0-0.1 |
| Dioxopiperazine | 0-4 |
| Purity (GC) | 95-100 |
| Appearance | White To Off-White Powder |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿320.00 |
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| 5.000 | 10-20 days | ฿760.00 |
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| 25.000 | 10-20 days | ฿2,420.00 |
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| 100.000 | 10-20 days | ฿7,690.00 |
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4-Ethyl-2,3-dioxo-1-piperazine carbonyl chloride
This compound is primarily utilized in the synthesis of various pharmaceutical intermediates, particularly in the development of antibiotics and other therapeutic agents. Its reactive carbonyl chloride group makes it a valuable building block in organic synthesis, enabling the formation of amide bonds with amines or other nucleophiles. It is often employed in the preparation of piperazine derivatives, which are key structural components in many drugs targeting bacterial infections, central nervous system disorders, and cardiovascular diseases. Additionally, its use in peptide coupling reactions is significant for creating complex molecular structures in medicinal chemistry. The compound's versatility and reactivity make it a crucial reagent in the production of biologically active molecules.
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