1-(tert-Butoxycarbonyl)-1,2,3,6-tetrahydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine TCI B4051

Chemical Identity

CAS No.: 286961-14-6
PubChem: CID 4642098·SID 253660227
Formula: C16H28BNO4
Molecular weight: 309.2 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-1-carboxylate
SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CCN(CC2)C(=O)OC(C)(C)C
InChIKey: VVDCRJGWILREQH-UHFFFAOYSA-N

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This compound, TCI B4051, is an organoboron reagent with a complex molecular structure containing both a tert-butoxycarbonyl group and a boron-containing group. It plays a crucial role in organic chemistry laboratories, particularly in the synthesis of heterocyclic compounds and coupling reactions. Its unique chemical structure enables it to participate in various organoboron reactions, making it a valuable tool for chemists working on complex molecular transformations. The compound's versatility allows it to be used in multiple synthetic pathways, contributing to the development of new chemical entities with specific functional properties.

The compound's properties, including its reactivity and selectivity, make it a preferred choice for advanced synthetic applications. It is known for its stability under controlled conditions and its ability to undergo reactions such as Suzuki-Miyaura and Kumada-Corriu. These characteristics make it suitable for applications requiring high precision and controlled chemical environments. Its ability to act as a reagent in organoboron chemistry also supports the synthesis of aromatic and heterocyclic compounds, which are essential in pharmaceutical and materials science research.

In Indonesian laboratories, this compound is widely used in organic chemistry research, especially in the fields of pharmacology and the synthesis of bioactive compounds. It is an essential component of the laboratory toolkit, supporting scientific innovation and technological advancement in educational and research institutions. Its presence in these settings underscores its importance in the development of new chemical methodologies and applications.

TCI brochures (PDF)

Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 17
Boron Compounds 2025-10-07 · p. 15

Related TCI products

Organic synthesis of heterocyclic compounds due to its reactivity and selectivity in coupling reactions.
Pharmaceutical research for the development of bioactive molecules through complex synthetic pathways.
Advanced chemical reactions such as Suzuki-Miyaura and Kumada-Corriu in organic chemistry laboratories.
Synthesis of aromatic compounds where organoboron reagents are required for high precision and control.
Supporting research in bioactive compound development by enabling the creation of structurally complex molecules.

Brand	TCI
CAS number	286961-14-6
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

This compound should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which could affect its chemical integrity. Proper ventilation is essential when handling the material to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. The compound should be stored away from incompatible substances to prevent any potential chemical interactions. Regular monitoring of storage conditions is advised to ensure optimal performance and safety in laboratory settings.

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