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TCI

CAS 635305-24-7

5-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene TCI C3301

5-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene TCI C3301
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Description

5-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene is a specialized chemical compound widely used in organic chemistry laboratories. It plays a crucial role in various synthetic processes, particularly in the development of heterocyclic compounds. This reagent is essential for facilitating coupling reactions, such as S-N coupling and the Suzuki-Miyaura reaction, which are fundamental in the synthesis of complex organic molecules. Its unique structure, incorporating both boron and chlorine functionalities, makes it a versatile tool in modern chemical research.

The compound's chemical properties, including its reactivity and stability under controlled conditions, make it a preferred choice for researchers. Its ability to participate in multiple reaction pathways enhances its utility in synthetic chemistry. The presence of the boronic acid group allows it to act as a key intermediate in cross-coupling reactions, which are vital for the creation of new compounds with specific biological or material properties. This reagent is especially valuable in applications requiring high selectivity and efficiency.

In Indonesian laboratories, this compound is commonly used in pharmaceutical and materials science research. It is an essential component in the development of new drugs and advanced materials. Due to its complex molecular structure, it is often employed in studies aimed at understanding and improving the reactivity of organic compounds. Its application is widespread in academic and industrial settings, contributing to the advancement of scientific knowledge and innovation.

Laboratory Applications

  • Used in pharmaceutical research for the synthesis of bioactive compounds due to its reactivity in coupling reactions.
  • Applied in materials science for the development of new polymers and functional materials through cross-coupling processes.
  • Employed in synthetic organic chemistry for the preparation of heterocyclic compounds with specific structural features.
  • Utilized in academic research for exploring new reaction mechanisms and synthetic pathways in organic chemistry.
  • Integrated into drug discovery programs to facilitate the construction of complex molecular frameworks with therapeutic potential.

Specifications

  • Brand: TCI
  • CAS number: 635305-24-7
  • Category: Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
  • Pack sizes: Available in various quantities as per supplier specifications
  • Physical form: Solid or liquid, depending on the specific formulation
  • Storage note: Requires dry and cool storage to prevent moisture and oxidation

Handling and Storage

This compound should be stored in a dry, cool environment away from moisture and oxidizing agents to maintain its chemical stability. It is recommended to use airtight containers made of inert materials such as glass or polyethylene to prevent exposure to humidity. Due to its sensitivity to moisture, handling should be done in a controlled atmosphere with appropriate safety measures. The compound should be kept in a well-ventilated area to minimize the risk of inhalation. Proper labeling and storage conditions are essential to ensure the integrity and safety of the material during laboratory use. Always follow standard laboratory safety protocols when working with this reagent.

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