5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole TCI I0590

Chemical Identity

CAS No.: 269410-24-4
PubChem: CID 2734772·SID 87560375
Formula: C14H18BNO2
Molecular weight: 243.11 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC3=C(C=C2)NC=C3
InChIKey: FATPQDPUKVVCLT-UHFFFAOYSA-N

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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole is a specialized chemical compound used in organic laboratory settings for its unique reactivity and structural versatility. This organoboron compound plays a crucial role in synthetic chemistry, particularly in the development of complex molecular structures. Its presence in various organic reactions allows chemists to achieve high levels of precision and control in their experiments. Due to its functional group, it is especially valuable in reactions that require the introduction of boron-based functionalities.

The compound is favored for its stability under controlled conditions and its ability to participate in a wide range of chemical transformations. The boron-containing group enhances its reactivity in coupling reactions, making it an essential reagent in modern synthetic strategies. Its compatibility with different reaction conditions and solvents further contributes to its widespread use. The compound’s molecular structure ensures it remains effective in both industrial and academic research environments.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in the synthesis of pharmaceuticals and industrial chemicals. Its role in creating complex heterocyclic structures is vital for drug development and material science applications. The compound’s reliability and performance make it a preferred choice for researchers requiring high-quality reagents for advanced chemical processes.

TCI brochures (PDF)

Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 17
Boron Compounds 2025-10-07 · p. 19

Related TCI products

Suzuki-Miyaura Coupling Reactions: This compound is ideal for coupling reactions due to its boron functionality, enabling efficient cross-coupling with aryl halides to form complex heterocyclic structures.
Organic Synthesis of Pharmaceuticals: Its reactivity and stability make it a key reagent in the synthesis of bioactive compounds, supporting drug development efforts.
Industrial Chemical Production: Used in the creation of specialty chemicals, it contributes to the production of materials with specific functional properties.
Heterocyclic Compound Synthesis: The compound’s structure facilitates the formation of various heterocyclic rings, essential in both academic and industrial research.
Advanced Organic Reaction Studies: Its versatility supports a wide range of chemical transformations, making it suitable for research into new synthetic methodologies.

Brand	TCI
CAS number	269410-24-4
Molecular formula	—
Purity	—
Category	Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes	Available in various quantities as per standard laboratory reagent packaging
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 chemical integrity and prevent degradation. It is recommended to use airtight containers to protect it from moisture and air exposure. Due to its organoboron nature, it should be handled with care to avoid any potential reactivity with incompatible substances. Proper labeling and storage in a designated chemical storage area are essential for safety. Always ensure that the workspace is well-ventilated when handling this material. Regular inspection of storage conditions is advised to maintain optimal performance and safety standards in the laboratory.

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