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CAS 141091-37-4

2-(1-Cyclohexenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane TCI C2707

2-(1-Cyclohexenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane TCI C2707

Chemical Identity

Other names
1-Cyclohexeneboronic Acid Pinacol Ester · 1-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohexene
CAS No.
141091-37-4
PubChem
CID 10932675·SID 172089043
Formula
C12H21BO2
Molecular weight
208.11 g/mol
Purity
>95.0%(GC)
Storage
0-10°C
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-(cyclohexen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
SMILES
B1(OC(C(O1)(C)C)(C)C)C2=CCCCC2
InChIKey
QNZFUMVTUFOLRT-UHFFFAOYSA-N
MDL
MDL05663845
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2-(1-Cyclohexenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound widely used in modern organic synthesis. This reagent plays a crucial role in catalytic reactions, particularly in coupling reactions such as the Suzuki-Miyaura reaction. Its ability to facilitate the formation of complex molecules from simpler ones makes it indispensable in chemical laboratories. It is especially valuable for the synthesis of heterocyclic compounds and complex organic structures, which are common in pharmaceutical and materials research.

The compound’s unique molecular structure, containing a cyclohexene ring and a boron atom, contributes to its versatility in chemical reactions. Its stability under certain conditions and compatibility with transition metals like palladium make it a preferred choice for catalytic processes. Additionally, its capacity to undergo both electrophilic and nucleophilic activation allows it to be applied in a wide range of synthetic strategies. These properties make it a reliable and effective reagent for advanced chemical applications.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, pharmaceutical compound synthesis, and the development of new chemical materials. Its catalytic efficiency and broad applicability have made it a sought-after reagent among researchers and laboratories focused on innovation in chemical science. Its role in facilitating complex molecular transformations supports ongoing advancements in both academic and industrial chemical research.

TCI brochures (PDF)

  • Suzuki-Miyaura Coupling Reactions: This compound is ideal for coupling reactions due to its ability to activate and stabilize transition metal catalysts, enhancing reaction efficiency and selectivity.
  • Synthesis of Heterocyclic Compounds: Its molecular structure enables the formation of complex ring systems, making it valuable in the creation of pharmaceutical and functional materials.
  • Organic Chemistry Research: It supports a wide range of synthetic strategies, contributing to the development of new chemical compounds and molecular architectures.
  • Pharmaceutical Compound Development: Its role in catalytic processes aids in the synthesis of bioactive molecules, supporting drug discovery and development efforts.
  • Material Science Applications: It is used in the synthesis of advanced materials, contributing to the creation of polymers and other functional chemical substances.

Brand TCI
CAS number 141091-37-4
Molecular formula —
Purity —
Category Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes As per supplier specifications
Physical form Liquid
Storage Store in a cool, dry place away from light and incompatible substances

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use sealed, airtight containers to prevent exposure to moisture and air. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that it is stored separately from strong oxidizing agents and reactive materials to avoid any potential chemical interactions. Proper labeling and storage conditions help maintain its stability and effectiveness in laboratory applications.

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