• (5-Formylthiophen-3-yl)boronic Acid (contains varying amounts of Anhydride) (CAS 175592-59-3) - TCI F1065 - AMI Scientific
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TCI

CAS 175592-59-3

(5-Formylthiophen-3-yl)boronic Acid (contains varying amounts of Anhydride) TCI F1065

(5-Formylthiophen-3-yl)boronic Acid (contains varying amounts of Anhydride) TCI F1065
Rp 6.817.650,00
Rp 6.817.650,00
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(5-Formylthiophen-3-yl)boronic Acid is a versatile organic compound widely used in laboratory settings for its role in various synthetic reactions. It serves as a key reagent in the synthesis of heterocyclic compounds and complex molecular structures, making it essential for advanced chemical research. This compound is particularly valuable in the field of organoboron chemistry, where it contributes to the development of new materials and pharmaceutical compounds. Its unique chemical properties allow it to participate in multiple reaction pathways, enhancing its utility across different experimental applications.

The compound is known for its high reactivity and ability to form stable bonds with organic ligands and metals. These properties make it a preferred choice for reactions such as the Suzuki-Miyaura and Heck coupling reactions, which are fundamental in organic synthesis. Its stability under certain conditions ensures reliable results, making it a trusted reagent in both academic and industrial laboratories. The combination of reactivity and stability allows researchers to achieve precise and consistent outcomes in their experiments.

In Indonesian laboratories, (5-Formylthiophen-3-yl)boronic Acid is commonly used in organic chemistry research, especially in the synthesis of complex compounds and drug development. Its availability and reliability make it a staple in chemical laboratories, supporting a wide range of experimental needs. The compound's role in creating new molecular structures underscores its importance in advancing scientific research in Indonesia.

  • Organic synthesis of heterocyclic compounds due to its reactivity and ability to form stable bonds with various ligands.
  • Use in Suzuki-Miyaura coupling reactions for efficient cross-coupling of aryl halides with boronic acids.
  • Application in Heck reactions for the formation of carbon-carbon bonds in complex molecule synthesis.
  • Support in the development of pharmaceutical compounds through its role in creating boron-containing structures.
  • Utilization in material science research for the synthesis of advanced polymers and functional materials.

Brand TCI
CAS number 175592-59-3
Molecular formula —
Purity —
Category Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes Varies as per supplier
Physical form Solid
Storage Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep it in a sealed container to avoid exposure to moisture, which can affect its reactivity. Due to its chemical nature, it should be handled in a well-ventilated area to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the material. Proper disposal methods should be followed to ensure compliance with environmental and safety regulations. The compound is not classified as hazardous under standard laboratory conditions, but standard chemical safety protocols should still be observed.

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