Ethyl 5-bromo-1H-imidazole-4-carboxylate

97%

  • Product Code: 124386
  CAS:    944906-76-7
Molecular Weight: 219.04 g./mol Molecular Formula: C₆H₇BrN₂O₂
EC Number: MDL Number: MFCD10697506
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, inert atmosphere
Product Description: Ethyl 5-bromo-1H-imidazole-4-carboxylate is primarily utilized in the synthesis of various pharmaceutical compounds, particularly those involving imidazole derivatives. It serves as a key intermediate in the development of drugs targeting neurological disorders, infections, and inflammatory conditions. The compound is also employed in organic synthesis to create complex molecules for research purposes, including the study of enzyme inhibition and receptor binding. Its bromo and ester functional groups make it a versatile building block in medicinal chemistry, enabling the introduction of specific modifications to enhance drug efficacy and selectivity. Additionally, it finds application in the preparation of agrochemicals, contributing to the creation of pesticides and herbicides with improved activity and stability.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $491.81
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0.250 10-20 days $835.36
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1.000 10-20 days $2,254.75
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Ethyl 5-bromo-1H-imidazole-4-carboxylate
Ethyl 5-bromo-1H-imidazole-4-carboxylate is primarily utilized in the synthesis of various pharmaceutical compounds, particularly those involving imidazole derivatives. It serves as a key intermediate in the development of drugs targeting neurological disorders, infections, and inflammatory conditions. The compound is also employed in organic synthesis to create complex molecules for research purposes, including the study of enzyme inhibition and receptor binding. Its bromo and ester functional groups make it a versatile building block in medicinal chemistry, enabling the introduction of specific modifications to enhance drug efficacy and selectivity. Additionally, it finds application in the preparation of agrochemicals, contributing to the creation of pesticides and herbicides with improved activity and stability.
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