tert-Butyl (4-bromo-2-cyano-1H-pyrrol-1-yl)carbamate

≥95%

  • Product Code: 80487
  CAS:    937047-04-6
Molecular Weight: 286.13 g./mol Molecular Formula: C₁₀H₁₂BrN₃O₂
EC Number: MDL Number: MFCD15142762
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, dry and sealed
Product Description: This chemical is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. It is particularly valuable in the construction of pyrrole-based compounds, which are often explored for their biological activity. The presence of both a bromo and a cyano group allows for further functionalization, making it a versatile building block in medicinal chemistry. Researchers often employ it in the synthesis of potential drug candidates, especially those targeting enzymes or receptors where pyrrole derivatives show affinity. Its tert-butyl carbamate group provides stability during reactions, ensuring the integrity of the pyrrole core while allowing for selective deprotection when needed. This compound is also used in the study of heterocyclic chemistry, contributing to the development of novel materials or catalysts.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿11,169.00
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-
0.250 10-20 days ฿22,338.00
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tert-Butyl (4-bromo-2-cyano-1H-pyrrol-1-yl)carbamate
This chemical is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. It is particularly valuable in the construction of pyrrole-based compounds, which are often explored for their biological activity. The presence of both a bromo and a cyano group allows for further functionalization, making it a versatile building block in medicinal chemistry. Researchers often employ it in the synthesis of potential drug candidates, especially those targeting enzymes or receptors where pyrrole derivatives show affinity. Its tert-butyl carbamate group provides stability during reactions, ensuring the integrity of the pyrrole core while allowing for selective deprotection when needed. This compound is also used in the study of heterocyclic chemistry, contributing to the development of novel materials or catalysts.
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