1-(tert-Butoxycarbonyl)indole-2-boronic Acid (contains varying amounts of Anhydride) TCI B5145

Chemical Identity

CAS No.: 213318-44-6
PubChem: CID 2773302·SID 468590545
Formula: C13H16BNO4
Molecular weight: 261.08 g/mol
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: [1-[(2-methylpropan-2-yl)oxycarbonyl]indol-2-yl]boronic acid
SMILES: B(C1=CC2=CC=CC=C2N1C(=O)OC(C)(C)C)(O)O
InChIKey: SVIBPSNFXYUOFT-UHFFFAOYSA-N

Rp 2.464.350,00

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1-(tert-Butoxycarbonyl)indole-2-boronic Acid is a specialized chemical compound used in organic synthesis, particularly in the preparation of heterocyclic compounds and boronic acid derivatives. This reagent plays a crucial role in laboratory settings where complex molecular structures need to be synthesized with high precision. Its unique chemical structure, containing both boronic acid and tert-butoxycarbonyl groups, makes it a valuable tool for chemists working on advanced synthetic routes. The compound is known for its versatility in various reaction conditions, allowing for the formation of diverse chemical entities with controlled reactivity.

The compound's reactivity is enhanced by the presence of varying amounts of anhydride, which contributes to its effectiveness in coupling reactions. This property allows it to participate in a wide range of organic transformations, including substitution and addition reactions. Its ability to react with both nucleophilic and electrophilic reagents makes it a preferred choice for researchers aiming to develop new synthetic methodologies. The presence of anhydride also increases its potential for use in more complex synthetic applications, expanding its utility in the field of organoboron chemistry.

In Indonesian laboratories, this compound is widely used by chemists and researchers in the field of organic synthesis. Its availability and adherence to international quality standards make it a reliable choice for both academic and industrial research. The compound is particularly favored for its role in the synthesis of indole-based compounds, which are important in pharmaceutical and materials science research. Its application continues to grow as more studies explore its potential in advanced chemical processes.

TCI brochures (PDF)

Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 14

Related TCI products

Organic synthesis of heterocyclic compounds due to its ability to participate in coupling reactions and form stable intermediates.
Preparation of boronic acid derivatives through controlled chemical transformations involving nucleophilic and electrophilic reagents.
Synthesis of indole-based molecules, which are essential in pharmaceutical and medicinal chemistry applications.
Development of new synthetic methodologies in organoboron chemistry due to its reactivity and structural versatility.
Research in materials science where complex molecular structures are required for advanced functional materials.

Brand	TCI
CAS number	213318-44-6
Molecular formula	—
Purity	—
Category	Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes	—
Physical form	—
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, which can affect its reactivity. Due to its potential reactivity with various reagents, it should be handled in a well-ventilated laboratory setting. Proper personal protective equipment, including gloves and safety goggles, should be worn when handling this material. Avoid contact with incompatible substances to ensure safety during storage and use. Regular monitoring of storage conditions is advised to maintain optimal performance and safety standards in the laboratory.

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