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Catalog Number:
44996
CAS Number:
5751-83-7
Ethyl 5-bromothiophene-2-carboxylate
Purity:
≥ 98% (GC)
Synonym(s):
5-Bromothiophene-2-carboxylic acid ethyl ester
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Product Information

Ethyl 5-bromothiophene-2-carboxylate is a versatile compound widely utilized in organic synthesis and pharmaceutical research. This compound features a bromine atom that enhances its reactivity, making it an excellent building block for the development of various bioactive molecules. Its unique structure allows for applications in the synthesis of thiophene derivatives, which are crucial in the production of agrochemicals, dyes, and advanced materials. Researchers often leverage its properties to create novel compounds with potential applications in medicinal chemistry, particularly in the development of anti-inflammatory and anti-cancer agents.

In addition to its synthetic utility, Ethyl 5-bromothiophene-2-carboxylate stands out for its ease of functionalization, allowing chemists to modify its structure to tailor specific properties for targeted applications. Its compatibility with various reaction conditions makes it a preferred choice for both academic and industrial laboratories. This compound not only streamlines the synthesis process but also enhances the efficiency of developing new chemical entities, making it an essential addition to any research portfolio.

Synonyms
5-Bromothiophene-2-carboxylic acid ethyl ester
CAS Number
5751-83-7
Purity
≥ 98% (GC)
Molecular Formula
C7H7BrO2S
Molecular Weight
235.1
MDL Number
MFCD02683089
PubChem ID
605723
Density
1.55
Appearance
Light orange to yellow to green clear liquid
Boiling Point
175 °C
Refractive Index
n20D 1.56
Conditions
Store at RT
General Information
Synonyms
5-Bromothiophene-2-carboxylic acid ethyl ester
CAS Number
5751-83-7
Purity
≥ 98% (GC)
Molecular Formula
C7H7BrO2S
Molecular Weight
235.1
MDL Number
MFCD02683089
PubChem ID
605723
Density
1.55
Appearance
Light orange to yellow to green clear liquid
Boiling Point
175 °C
Refractive Index
n20D 1.56
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ethyl 5-bromothiophene-2-carboxylate is widely utilized in research focused on:

  • Synthetic Organic Chemistry: This compound serves as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, enabling researchers to create complex molecular structures efficiently.
  • Material Science: It is used in the development of organic semiconductors, contributing to advancements in electronic devices such as organic light-emitting diodes (OLEDs) and solar cells.
  • Medicinal Chemistry: The compound is explored for its potential biological activities, including anti-inflammatory and antimicrobial properties, making it a candidate for new drug development.
  • Polymer Chemistry: Ethyl 5-bromothiophene-2-carboxylate can be incorporated into polymer matrices, enhancing material properties for applications in coatings and adhesives.
  • Research and Development: Its unique chemical structure allows for modifications that can lead to the discovery of novel compounds, addressing specific challenges in various fields such as agriculture and medicine.

Citations