4-Methyl-2-thiopheneboronic Acid (contains varying amounts of Anhydride) TCI M2840

Chemical Identity

CAS No.: 162607-15-0
PubChem: CID 2734373·SID 354335383
Formula: C5H7BO2S
Molecular weight: 141.99 g/mol
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (4-methylthiophen-2-yl)boronic acid
SMILES: B(C1=CC(=CS1)C)(O)O
InChIKey: DFUMIZDUIJNUJU-UHFFFAOYSA-N

Rp 1.458.450,00

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4-Methyl-2-thiopheneboronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of heterocyclic compounds and coupling reactions. This reagent plays a crucial role in laboratory settings where the formation of new chemical bonds is required. Its unique structure, containing both boronic acid and thiophene groups, enhances its reactivity under various chemical conditions. This versatility makes it an essential component in the toolkit of chemists working in diverse research fields.

The compound's reactivity is further enhanced by the presence of varying amounts of anhydride, which provides flexibility in its application. This characteristic allows it to participate in a wide range of reactions, including those involving different ligands and metals. Its ability to interact with various organic compounds makes it a preferred choice for researchers aiming to develop new materials, pharmaceuticals, and environmental chemicals. The compound's chemical complexity ensures that it remains a valuable asset in modern synthetic chemistry.

In Indonesian laboratories, 4-Methyl-2-thiopheneboronic Acid is commonly used in organic chemistry research, especially in the fields of pharmacy, materials science, and environmental chemistry. Its role in catalytic reactions and synthetic pathways has made it a staple in both academic and industrial research environments. The compound's adaptability and reactivity continue to drive innovation in chemical synthesis and development.

TCI brochures (PDF)

Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 14
Boron Compounds 2025-10-07 · p. 14
Building Blocks for Organic Semiconductor 2026-03-24 · p. 26

Related TCI products

Organic synthesis is a key application where this reagent is used for coupling reactions and heterocyclic compound formation due to its reactivity and structural versatility.
Pharmaceutical research benefits from its ability to participate in complex synthetic pathways, aiding in the development of new drug molecules and therapeutic agents.
Materials science applications rely on its reactivity to create novel polymers and functional materials with specific chemical properties.
Environmental chemistry studies utilize it for the synthesis of compounds used in pollution control and remediation processes.
Academic research in Indonesia frequently employs this compound to explore new chemical reactions and synthetic methodologies in both undergraduate and postgraduate studies.

Brand	TCI
CAS number	162607-15-0
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. Due to its reactivity, it should be handled with care in a well-ventilated laboratory setting. Proper personal protective equipment, such as gloves and safety goggles, should be worn during handling. Avoid contact with incompatible substances to ensure safe usage. Regular monitoring of storage conditions is advised to maintain optimal performance and safety in laboratory applications.

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