Methyl 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate TCI M2665

Chemical Identity

CAS No.: 480425-35-2
PubChem: CID 2734651·SID 253662469
Formula: C14H19BO4
Molecular weight: 262.11 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: methyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC(=CC=C2)C(=O)OC
InChIKey: JBJGSVBGUBATNH-UHFFFAOYSA-N

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TCI M2665 480425-35-2 Methyl 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate is a specialized organoboron compound widely used in organic chemistry laboratories. This reagent plays a crucial role in various synthetic processes, particularly in the formation of aromatic and heterocyclic compounds. Its unique structure, featuring a boron-containing group attached to a benzoate chain, allows it to participate in a range of chemical reactions, including coupling and substitution reactions. Due to its versatility and reactivity, it is a valuable tool for researchers working on complex molecule synthesis.

The compound is favored for its stable molecular structure and controlled reactivity, which make it reliable for precise chemical applications. The presence of the boron group enables it to form stable complexes with various ligands, enhancing its utility in diverse chemical transformations. Its predictable behavior under different reaction conditions ensures consistent results, making it a preferred choice in both academic and industrial research settings. This stability and reactivity are essential for maintaining the integrity of chemical processes in laboratory environments.

In Indonesian laboratories, this compound is commonly used in pure and applied chemistry research, especially in pharmaceutical, material science, and catalysis fields. Its ability to participate in controlled chemical reactions makes it an essential reagent for developing new compounds and materials. Researchers rely on its performance to achieve accurate and reproducible outcomes in their experiments, contributing to advancements in scientific research across multiple disciplines.

TCI brochures (PDF)

Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 16
Boron Compounds 2025-10-07 · p. 16

Related TCI products

Organic synthesis applications benefit from this reagent's ability to participate in coupling reactions, enabling the formation of complex aromatic and heterocyclic structures with high efficiency.
Pharmaceutical research utilizes this compound due to its capacity to form stable boron-based intermediates, which are crucial in the development of new drug molecules and therapeutic agents.
Material science applications leverage its reactivity to create advanced polymers and functional materials with tailored chemical properties and structural integrity.
Catalytic processes benefit from its ability to act as a versatile organoboron reagent, enhancing reaction efficiency and selectivity in various synthetic pathways.
Analytical chemistry uses this compound as a reference standard for characterizing and quantifying boron-containing compounds in complex mixtures.

Brand	TCI
CAS number	480425-35-2
Molecular formula	—
Purity	—
Category	Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes	Available in standard laboratory quantities as per supplier specifications
Physical form	Solid or liquid, depending on formulation and supplier packaging
Storage	—

This compound should be stored in a cool, dry, and well-ventilated area away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid exposure to incompatible substances, and ensure proper ventilation when working with this reagent. Regular monitoring of storage conditions is advised to maintain its stability and effectiveness in chemical reactions.

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