4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine TCI M3231

Chemical Identity

CAS No.: 1171891-31-8
PubChem: CID 57370080·SID 468592353
Formula: C12H18BNO2
Molecular weight: 219.09 g/mol
Purity: >98.0%(GC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
SMILES: B1(OC(C(O1)(C)C)(C)C)C2=C(C=CN=C2)C
InChIKey: GZYZXNXJTPRMKF-UHFFFAOYSA-N

Rp 2.254.350,00

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

4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a chemical compound widely used in organometallic reactions, particularly in the synthesis of heterocyclic compounds and boron derivatives. This reagent plays a crucial role in modern synthetic chemistry, especially in reactions that require precise control over molecular structure. It is a key component in the development of complex molecules, making it an essential tool for researchers working in advanced organic chemistry. Its application spans various fields, including pharmaceutical and materials science, where the ability to form stable intermediates is vital.

The compound is favored for its stability under controlled laboratory conditions and its ability to form stable bonds with metals such as palladium. These properties make it highly effective in coupling reactions like Suzuki and Kumada, which are essential for creating complex molecular architectures. Its chemical structure allows for high reactivity and selectivity, ensuring efficient and reproducible results in synthetic processes. Additionally, its non-toxic nature in controlled environments makes it a preferred choice for laboratories seeking safe and reliable reagents.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, especially by academic institutions and research centers focused on molecular synthesis. Its role in developing new synthetic techniques and creating functional compounds makes it a valuable resource for both educational and industrial applications. The compound’s versatility and reliability contribute to its widespread use in the scientific community.

TCI brochures (PDF)

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

Related TCI products

Used in the synthesis of heterocyclic compounds due to its ability to form stable boron-containing intermediates.
Applied in Suzuki coupling reactions to facilitate the formation of carbon-carbon bonds with high efficiency.
Utilized in pharmaceutical research for the development of complex drug molecules requiring precise structural control.
Employed in materials science for the creation of advanced polymers and functional materials.
Integrated into academic research programs to support the training of students in modern synthetic methodologies.

Brand	TCI
CAS number	1171891-31-8
Molecular formula	—
Purity	—
Category	Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes	Available in various quantities as per standard laboratory supply practices.
Physical form	Solid or liquid, depending on formulation and supplier specifications.
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 stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air, which can affect its reactivity. Proper labeling of storage containers is essential for safety and traceability. In laboratory settings, it should be handled with standard chemical safety protocols, including the use of personal protective equipment such as gloves and goggles. Although it is considered non-toxic in controlled environments, it is still important to follow general laboratory safety practices to ensure safe handling and storage.

—