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 $9.60
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5.000 10-20 days $22.80
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25.000 10-20 days $72.61
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100.000 10-20 days $230.72
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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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