• 478706-06-8 9-n-Octyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole - AMI Scientific
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TCI

CAS 478706-06-8

9-n-Octyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole TCI O0497

9-n-Octyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole TCI O0497

Chemical Identity

CAS No.
478706-06-8
PubChem
CID 58121526·SID 354335333
Formula
C32H47B2NO4
Molecular weight
531.3 g/mol
Purity
>98.0%(HPLC)(N)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
9-octyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)carbazole
SMILES
B1(OC(C(O1)(C)C)(C)C)C2=CC3=C(C=C2)N(C4=C3C=C(C=C4)B5OC(C(O5)(C)C)(C)C)CCCCCCCC
InChIKey
VWWIAQNEZFWMFK-UHFFFAOYSA-N
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9-n-Octyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole is a complex organoboron compound widely used in advanced chemical reactions, particularly in organic synthesis. This reagent plays a crucial role in laboratory settings where precision and controlled reactivity are essential. Its unique structure enables it to participate in various coupling reactions, such as Suzuki and Stille, which are fundamental in the creation of heterocyclic compounds and complex molecular architectures. The presence of boronic acid functionalities makes it a versatile tool for synthetic chemists.

The compound’s molecular design, featuring a carbazole core with two boronic acid groups, provides it with high reactivity and specificity. The n-octyl chain enhances its hydrophobic properties, improving solubility in organic solvents and facilitating its use in a wide range of reaction conditions. These characteristics make it a preferred choice for researchers aiming to achieve controlled and efficient synthetic outcomes. Its stability under specific reaction conditions further supports its reliability in laboratory applications.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, drug development, and the synthesis of complex molecules. Its ability to participate in selective coupling reactions makes it an essential reagent for scientists working on advanced synthetic pathways. Due to its specialized properties, it is a key component in many research projects aimed at creating new chemical entities with specific structural and functional features.

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  • Drug development involves the synthesis of complex molecules, where this compound's reactivity and selectivity are crucial for creating novel pharmaceutical compounds.
  • Organic synthesis requires precise reagents that can participate in coupling reactions, making this compound ideal for constructing heterocyclic structures.
  • Heterocyclic compound synthesis benefits from the compound's ability to form stable intermediates, enhancing the efficiency of multi-step synthetic processes.
  • Advanced chemical research relies on reagents with controlled reactivity, and this compound provides the necessary functionality for such studies.
  • Molecular complexity studies utilize this compound to explore the behavior of boronic acid groups in various chemical environments.

Brand TCI
CAS number 478706-06-8
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 light

This compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its organoboron nature, it is important to handle it with care, using appropriate personal protective equipment. Storage away from incompatible materials is essential to ensure safety. Proper labeling of containers is required for easy identification and safe handling. Regular inspection of storage conditions is advised to maintain optimal reagent quality.

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