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Catalog Number:
23989
CAS Number:
1015856-43-5
Tert-Butyl 2-(Dibromomethyl)Quinoline-4-Carboxylate
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$236.05 /100MG
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Product Information

Tert-Butyl 2-(Dibromomethyl)Quinoline-4-Carboxylate is a versatile compound with significant applications in medicinal chemistry and organic synthesis. This compound features a unique quinoline structure, which is known for its biological activity, making it a valuable intermediate in the development of pharmaceuticals. Its dibromomethyl group enhances its reactivity, allowing for further functionalization, which is particularly beneficial in the synthesis of complex molecules. Researchers and industry professionals can leverage this compound in the design of novel drugs, especially in the fields of anti-cancer and anti-inflammatory agents, where quinoline derivatives have shown promising results.

Additionally, Tert-Butyl 2-(Dibromomethyl)Quinoline-4-Carboxylate stands out due to its stability and ease of handling, making it an ideal choice for laboratory settings. Its unique properties facilitate various reactions, including nucleophilic substitutions and coupling reactions, which are essential in the synthesis of advanced materials and biologically active compounds. With its potential to streamline synthetic pathways and enhance product yields, this compound is a valuable asset for any research or industrial application focused on innovative chemical solutions.

CAS Number
1015856-43-5
Molecular Formula
C15H15Br2NO2
Molecular Weight
401.1
MDL Number
MFCD09998273
PubChem ID
45926048
Conditions
Store at 0-8°C
General Information
CAS Number
1015856-43-5
Molecular Formula
C15H15Br2NO2
Molecular Weight
401.1
MDL Number
MFCD09998273
PubChem ID
45926048
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Tert-Butyl 2-(Dibromomethyl)Quinoline-4-Carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in developing anti-cancer agents due to its unique quinoline structure that enhances biological activity.
  • Material Science: It is used in creating advanced materials, including polymers and coatings, where its bromine content can improve flame retardancy and thermal stability.
  • Agricultural Chemistry: The compound is explored for its potential as a pesticide or herbicide, leveraging its chemical properties to target specific plant pathogens effectively.
  • Organic Synthesis: It acts as a versatile building block in organic chemistry, facilitating the creation of complex molecules through various reaction pathways, thus streamlining research processes.
  • Analytical Chemistry: This chemical is employed in analytical methods for detecting and quantifying quinoline derivatives in environmental samples, aiding in pollution monitoring and control.

Citations