2-Bromo-5-iodo-3-n-octylthiophene (stabilized with Copper chip) - 1085181-82-3

2-Bromo-5-iodo-3-n-octylthiophene (stabilized with Copper chip)

Catalog Number: EVT-2687301
CAS Number: 1085181-82-3
Molecular Formula: C12H18BrIS
Molecular Weight: 401.14
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Product Introduction

Description
2-Bromo-5-iodo-3-n-octylthiophene, stabilized with a Copper chip, is a chemical compound that has gained significant attention in various fields of research. This paper aims to provide a comprehensive overview of this compound, including its synthesis methods, chemical structure, biological activity, effects on cell function and signal transduction, applications in medical, environmental, and industrial research, as well as future perspectives and challenges.
Applications in Various Fields
In Medical Research, 2-Bromo-5-iodo-3-n-octylthiophene plays a crucial role in drug development. It has shown promising results in preclinical studies, demonstrating its potential as a therapeutic agent for various diseases. Clinical trials are underway to evaluate its efficacy and safety in humans. However, potential side effects and long-term effects need to be carefully monitored.
In Environmental Research, this compound has been studied for its effects on ecosystems. It plays a role in pollution management by acting as a catalyst for the degradation of harmful pollutants. Its use in sustainable environmental practices is being explored, with the aim of minimizing its environmental impact.
In Industrial Research, 2-Bromo-5-iodo-3-n-octylthiophene finds applications in manufacturing processes. It can improve product quality and efficiency in various industries, including electronics and materials science. Health and safety considerations are essential during its industrial use, and proper protocols must be followed to ensure worker safety.

Properties

CAS Number

1085181-82-3

Product Name

2-Bromo-5-iodo-3-n-octylthiophene (stabilized with Copper chip)

IUPAC Name

2-bromo-5-iodo-3-octylthiophene

Molecular Formula

C12H18BrIS

Molecular Weight

401.14

InChI

InChI=1S/C12H18BrIS/c1-2-3-4-5-6-7-8-10-9-11(14)15-12(10)13/h9H,2-8H2,1H3

InChI Key

WYOLKTBMZYMZBF-UHFFFAOYSA-N

SMILES

CCCCCCCCC1=C(SC(=C1)I)Br

Solubility

not available
Method of Synthesis or Extraction
Several methods are commonly used for the synthesis of 2-Bromo-5-iodo-3-n-octylthiophene. One such method involves the reaction of 2-bromo-5-iodothiophene with n-octylthiol in the presence of a copper catalyst. This method offers high efficiency and yield, with minimal environmental impact. Safety considerations include the use of appropriate protective equipment and adherence to proper handling and disposal protocols.
Chemical Structure and Biological Activity
The chemical structure of 2-Bromo-5-iodo-3-n-octylthiophene consists of a thiophene ring substituted with bromine, iodine, and an octyl group. This compound exhibits potent biological activity due to its ability to interact with specific biological targets. The mechanism of action involves modulation of signal transduction pathways, leading to various biological effects.
Biological Effects
The compound's effects on cell function and signal transduction are of particular interest. It has been found to influence cellular processes such as proliferation, differentiation, and apoptosis. Additionally, it can modulate various signaling pathways, including those involved in inflammation, cancer, and neurodegenerative diseases. However, further research is needed to fully understand its potential therapeutic and toxic effects.
Future Perspectives and Challenges
Despite the potential of 2-Bromo-5-iodo-3-n-octylthiophene, there are current limitations in its use and study. Further research is needed to fully understand its biological mechanisms and potential side effects. Challenges include optimizing synthesis methods, improving its stability, and developing targeted delivery systems.
Possible solutions and improvements include the development of novel synthesis techniques, exploring alternative stabilization methods, and enhancing its bioavailability. Future trends and prospects in the application of 2-Bromo-5-iodo-3-n-octylthiophene in scientific research include its integration into personalized medicine and the development of targeted therapies.
In conclusion, 2-Bromo-5-iodo-3-n-octylthiophene, stabilized with a Copper chip, is a compound with significant potential in various fields of research. Its synthesis methods, chemical structure, biological activity, effects on cell function, and applications in medical, environmental, and industrial research have been discussed. Future perspectives and challenges highlight the need for further research and improvements to fully harness its potential.

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