9-Phenylcarbazole-3-boronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of heterocyclic compounds. This versatile building block plays a crucial role in laboratory settings where complex molecular structures are being developed. Its unique chemical structure enables it to participate in various coupling reactions, making it an essential reagent for advanced synthetic pathways. This compound is commonly used in research and development projects that require precise molecular modifications.
The compound is valued for its chemical stability under controlled conditions and its reactivity with a range of reagents, including strong acids and alkali metals. Its ability to undergo coupling reactions, such as Suzuki or Kumada, makes it a preferred choice for chemists working on the synthesis of complex organic molecules. The presence of boronic acid functionality further enhances its utility in creating new compounds with tailored properties. These characteristics make it a reliable and efficient reagent in modern chemical laboratories.
In Indonesian laboratories, 9-Phenylcarbazole-3-boronic Acid is extensively used in organic chemistry research, especially in academic institutions and research centers. It is particularly relevant for projects focused on the synthesis of heterocyclic compounds and the development of new pharmaceuticals. Its application is widespread in both teaching and research environments, supporting the advancement of chemical sciences in the region.
TCI brochures (PDF)
- Carbazoles 2025-06-27 · p. 5
- Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 14
- Boron Compounds 2025-10-07 · p. 13
- Building Blocks for Organic Semiconductor 2026-03-24 · p. 21
Related TCI products
- TCI P2169 1001911-63-2 9-Phenylcarbazole-2-boronic Acid (contains varying amounts of Anhydride)
- TCI C2967 864377-33-3 3-(9H-Carbazol-9-yl)phenylboronic Acid (contains varying amounts of Anhydride)
- TCI C2926 419536-33-7 4-(9H-Carbazol-9-yl)phenylboronic Acid (contains varying amounts of Anhydride)
- TCI N1098 1133057-98-3 [9-(Naphthalen-2-yl)-9H-carbazol-3-yl]boronic Acid (contains varying amounts of Anhydride)
- TCI F0549 4347-33-5 5-Formyl-2-thiopheneboronic Acid (contains varying amounts of Anhydride)
- TCI E1153 669072-93-9 9-Ethylcarbazole-3-boronic Acid (contains varying amounts of Anhydride)
- Synthesis of Heterocyclic Compounds: This compound is ideal for creating complex ring structures, which are essential in pharmaceutical and material science research.
- Organic Coupling Reactions: Its boronic acid functionality makes it suitable for Suzuki and Kumada couplings, enabling the formation of new carbon-carbon bonds.
- Drug Development Projects: It is used in the design and synthesis of novel therapeutic agents, contributing to the discovery of new pharmaceutical compounds.
- Advanced Organic Chemistry Research: Its reactivity and structural versatility support cutting-edge research in synthetic chemistry and molecular design.
- Teaching and Learning in Chemistry: It is a valuable tool for demonstrating complex organic reactions and synthetic strategies in academic settings.
| Brand | TCI |
|---|---|
| CAS number | 854952-58-2 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Building Blocks > Heterocyclic Building Blocks |
| Pack sizes | As per supplier specifications |
| Physical form | Solid (as per standard product description) |
| 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 chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and air exposure. Due to its potential reactivity with strong acids and alkali metals, it should be handled with appropriate personal protective equipment. Keep the material away from incompatible substances to ensure safe laboratory practices. Regular monitoring of storage conditions is advised to maintain the integrity of the compound. Always follow standard safety protocols when working with reactive chemical building blocks.
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