Methyl 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate TCI M3057

Chemical Identity

CAS No.: 171364-80-0
PubChem: CID 2773500·SID 354335088
Formula: C14H19BO4
Molecular weight: 262.11 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

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

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Methyl 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate is a chemical compound widely used in organic reactions, particularly in the synthesis of complex molecules. As an organoboron reagent, it plays a crucial role in modern organic chemistry by enabling efficient and selective chemical transformations. This compound is especially valuable in laboratory settings where precision and control over reaction conditions are essential. Its unique structure allows it to participate in a variety of synthetic pathways, making it a versatile tool for researchers.

The compound's stability and controlled reactivity make it a preferred choice for laboratory applications. The presence of the boron group contributes to its ability to undergo specific reactions, such as coupling reactions, with high efficiency. Its compatibility with various reaction conditions ensures that it can be used in a wide range of synthetic strategies. These properties make it an essential component in the development of new compounds and materials.

In Indonesian laboratories, this reagent is commonly used by chemists and researchers working in organic synthesis, pharmaceutical development, and materials science. Its reliability and effectiveness in producing high-quality results make it a standard choice for both academic and industrial research. Its application in complex synthesis processes highlights its importance in advancing chemical research in the region.

TCI brochures (PDF)

Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 19

Related TCI products

Suzuki-Miyaura Coupling Reactions: This reagent is ideal for Suzuki-Miyaura coupling due to its stable boron group, which facilitates the formation of carbon-carbon bonds with high efficiency and selectivity.
Organic Synthesis of Aromatic Compounds: It is frequently used in the synthesis of aromatic compounds with various functional groups, offering versatility and reliability in reaction conditions.
Pharmaceutical Compound Development: Its role in creating complex molecular structures makes it a valuable tool in drug discovery and development processes.
Materials Science Research: It supports the creation of advanced materials by enabling precise chemical modifications and functional group incorporations.
Functional Group Modification: Its reactivity allows for the efficient modification of functional groups, making it suitable for a wide range of synthetic strategies.

Brand	TCI
CAS number	171364-80-0
Molecular formula	—
Purity	—
Category	Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes	Available in various sizes as per standard laboratory supply practices
Physical form	Solid or liquid, depending on the specific formulation
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 minimize exposure to moisture and air, which could affect its stability. Laboratory personnel should handle the material with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the storage area is well-ventilated to avoid any potential accumulation of volatile compounds. Proper labeling of containers is essential for safe handling and to prevent accidental exposure. Regular inspection of storage conditions ensures that the compound remains suitable for use in laboratory applications.

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