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Catalog Number:
24684
CAS Number:
712-52-7
2-bromo-2-(4-fluorophényl)acétate d'éthyle
Purity:
≥ 95% (CG)
Synonym(s):
Ester éthylique de l'acide bromo-(4-fluoro-phényl)-acétique
Documents
$72.31 /100 mg
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Product Information

Ethyl 2-bromo-2-(4-fluorophenyl)acetate is a versatile compound widely utilized in organic synthesis and pharmaceutical research. This compound features a unique combination of a bromo and a fluorophenyl group, making it an essential building block for the development of various biologically active molecules. Its reactivity allows for applications in the synthesis of complex organic compounds, particularly in the creation of pharmaceuticals and agrochemicals. Researchers appreciate its role in facilitating reactions such as nucleophilic substitutions and coupling reactions, which are crucial in drug discovery and development.

In addition to its synthetic utility, Ethyl 2-bromo-2-(4-fluorophenyl)acetate has shown potential in the development of novel therapeutic agents, particularly in targeting specific biological pathways. Its unique structural characteristics enable chemists to explore innovative pathways for drug design, enhancing the efficacy and specificity of new treatments. With its favorable properties and applications, this compound stands out as a valuable resource for researchers and industry professionals aiming to advance their projects in medicinal chemistry and related fields.

Synonyms
Ester éthylique de l'acide bromo-(4-fluoro-phényl)-acétique
CAS Number
712-52-7
Purity
≥ 95% (CG)
Molecular Formula
C10H10BrFO2
Molecular Weight
261.09
MDL Number
MFCD00204082
PubChem ID
2779786
Appearance
Liquide incolore à jaune
Boiling Point
120-130 °C / 5 mmHg
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Ester éthylique de l'acide bromo-(4-fluoro-phényl)-acétique
CAS Number
712-52-7
Purity
≥ 95% (CG)
Molecular Formula
C10H10BrFO2
Molecular Weight
261.09
MDL Number
MFCD00204082
PubChem ID
2779786
Appearance
Liquide incolore à jaune
Boiling Point
120-130 °C / 5 mmHg
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Ethyl 2-bromo-2-(4-fluorophenyl)acetate is widely utilized in research focused on:

  • Synthetic Organic Chemistry: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, allowing researchers to create complex molecules efficiently.
  • Medicinal Chemistry: It plays a crucial role in developing new drugs, particularly in creating compounds with enhanced biological activity and specificity, which can lead to more effective treatments.
  • Material Science: The compound is used in the formulation of specialty polymers and coatings, providing unique properties such as improved durability and resistance to environmental factors.
  • Fluorine Chemistry: Its fluorine atom enhances the compound's lipophilicity, making it valuable in designing agents for imaging and diagnostic applications in medical research.
  • Biochemical Research: Researchers utilize this compound to study enzyme interactions and metabolic pathways, contributing to a better understanding of biological processes and potential therapeutic targets.

Citations