Benzo[b]thiophene-3-boronic Acid (contains varying amounts of Anhydride) TCI B4774

Chemical Identity

CAS No.: 113893-08-6
PubChem: CID 2776344·SID 253660707
Formula: C8H7BO2S
Molecular weight: 178.02 g/mol
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 1-benzothiophen-3-ylboronic acid
SMILES: B(C1=CSC2=CC=CC=C12)(O)O
InChIKey: QVANIYYVZZLQJP-UHFFFAOYSA-N

Rp 1.272.600,00

~~Rp 905.100,00~~ Rp 1.272.600,00

Sale Sold out

Shipping calculated at checkout.

Berat 1g 5g

Pembayaran hanya melalui request quotation dan dilakukan setelah tim kami menghubungi Anda. Mohon cantumkan nomor WhatsApp aktif untuk konfirmasi pesanan & pembuatan invoice. Estimasi pengiriman 2-4 minggu setelah pembayaran.

Dokumen Keamanan & Mutu

↓ Unduh SDS / MSDS (PDF resmi TCI)

CoA (Certificate of Analysis)

Spesifik per batch produksi — diterbitkan dan dikirim bersama barang sesuai nomor lot yang Anda terima.

Contoh CoA segera tersedia.

💬 Minta CoA via WhatsApp

View full details

Benzo[b]thiophene-3-boronic Acid (TCI B4774) is a chemical compound widely used in organic reactions, particularly in the synthesis of complex molecules that require boron reactivity. This reagent plays a crucial role in laboratory settings, especially in the development of heterocyclic compounds and aromatic derivatives. Its unique structure and reactivity make it a valuable tool for chemists working on advanced synthetic pathways. The presence of varying amounts of anhydride further enhances its versatility in different reaction conditions.

The compound's properties, including its reactivity and molecular complexity, make it a preferred choice for specialized organic synthesis. Its ability to participate in coupling reactions such as Suzuki-Miyaura and Kumada-Corriu allows for the efficient construction of complex molecular frameworks. The presence of the boronic acid group provides a reactive site that can be modified under appropriate conditions, offering chemists a high degree of control over reaction outcomes. These characteristics make it an essential reagent in modern synthetic chemistry.

In Indonesian laboratories, Benzo[b]thiophene-3-boronic Acid is commonly used in organic chemistry research, especially in the synthesis of heterocyclic compounds and pharmaceutical development. Its reactivity and structural versatility make it a key component in projects requiring precise and controlled chemical transformations. Researchers in Indonesia rely on this compound for its reliability and effectiveness in complex synthetic processes.

TCI brochures (PDF)

Thiophenes 2026-06-29 · p. 11
Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 14
Boron Compounds 2025-10-07 · p. 12
Building Blocks for Organic Semiconductor 2026-03-24 · p. 27

Related TCI products

Organic synthesis of heterocyclic compounds due to its reactivity and structural versatility in coupling reactions.
Pharmaceutical development where precise chemical modifications are required for drug molecule construction.
Advanced synthetic pathways involving Suzuki-Miyaura and Kumada-Corriu reactions for complex molecule formation.
Research in aromatic derivative synthesis, leveraging its boronic acid functionality for functional group transformations.
Development of new chemical methodologies requiring stable and reactive organoboron reagents for controlled reactions.

Brand	TCI
CAS number	113893-08-6
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

Benzo[b]thiophene-3-boronic Acid should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep the compound in a sealed container to prevent exposure to moisture, which could affect its reactivity. Due to its reactive nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is advisable to store it in a well-ventilated area to minimize any potential risk of inhalation. Always ensure that the storage area is free from incompatible materials to avoid any unwanted chemical interactions. Proper handling and storage are essential to ensure the safety of laboratory personnel and the effectiveness of the reagent in experimental processes.

—