Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
25856
CAS Number:
399043-24-4
2-aminothiophén-3-yl)(4-bromophényl)méthanone
Purity:
≥ 98 % (HPLC)
Synonym(s):
2-Amino-3-(4-bromobenzoyl)thiophène
Documents
$75.00 /250 mg
Taille
Request Bulk Quote
Product Information

(2-Aminothiophen-3-yl)(4-bromophenyl)methanone is a versatile compound known for its significant applications in pharmaceutical research and development. This compound features a unique structure that combines a thiophene ring with a bromophenyl moiety, making it a valuable building block in the synthesis of various bioactive molecules. Its properties facilitate its use in the development of novel therapeutic agents, particularly in the fields of oncology and neurology, where it can serve as a precursor for compounds targeting specific biological pathways.

Researchers appreciate this compound for its potential to enhance drug efficacy and specificity, as well as its ability to undergo further functionalization. Its unique chemical properties allow for modifications that can lead to improved pharmacological profiles, making it an essential tool in medicinal chemistry. With its promising applications, (2-Aminothiophen-3-yl)(4-bromophenyl)methanone stands out as a key compound for professionals looking to innovate in drug discovery and development.

Synonyms
2-Amino-3-(4-bromobenzoyl)thiophène
CAS Number
399043-24-4
Purity
≥ 98 % (HPLC)
Molecular Formula
C11H8BrNOS
Molecular Weight
282.16
MDL Number
MFCD03118409
PubChem ID
859627
Melting Point
178-186 ?C
Appearance
Flocons jaunes
Conditions
Conserver à 0-8°C
General Information
Synonyms
2-Amino-3-(4-bromobenzoyl)thiophène
CAS Number
399043-24-4
Purity
≥ 98 % (HPLC)
Molecular Formula
C11H8BrNOS
Molecular Weight
282.16
MDL Number
MFCD03118409
PubChem ID
859627
Melting Point
178-186 ?C
Appearance
Flocons jaunes
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(2-Aminothiophen-3-yl)(4-bromophenyl)methanone is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting cancer and other diseases. Its unique structure allows for the modification of biological activity, making it a valuable asset in drug design.
  • Material Science: It is employed in the creation of advanced materials, such as organic semiconductors. These materials are crucial for developing efficient electronic devices, including solar cells and light-emitting diodes (LEDs).
  • Biochemical Research: Researchers use this compound to study enzyme interactions and metabolic pathways. Its ability to inhibit specific enzymes makes it a useful tool for understanding disease mechanisms and potential therapeutic targets.
  • Agricultural Chemistry: The compound has applications in developing agrochemicals, particularly in creating effective pesticides and herbicides. Its targeted action can help improve crop yields while minimizing environmental impact.
  • Analytical Chemistry: It is utilized as a standard reference material in analytical methods, aiding in the calibration of instruments and ensuring accurate measurements in various chemical analyses.

Citations