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CAS 10380-28-6

Bis(8-quinolinolato)copper(II) TCI B1677

Bis(8-quinolinolato)copper(II) TCI B1677

Chemical Identity

CAS No.
10380-28-6
PubChem
CID 3032555·SID 87564578
Formula
C18H12CuN2O2
Molecular weight
351.8 g/mol
Purity
>95.0%(T)
Reference databases
ChEBI·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
copper bis(quinolin-8-olate)
SMILES
C1=CC2=C(C(=C1)[O-])N=CC=C2.C1=CC2=C(C(=C1)[O-])N=CC=C2.[Cu+2]
InChIKey
YXLXNENXOJSQEI-UHFFFAOYSA-L
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Bis(8-quinolinolato)copper(II), with the CAS number 10380-28-6, is a chemical compound widely used in organic chemistry reactions, particularly in catalytic processes involving transition metals. This compound serves as an essential catalyst in cross-coupling reactions, where it facilitates the formation of carbon-carbon (C-C) bonds. Its role in the laboratory is critical for enabling efficient and selective chemical transformations, especially in synthetic routes that require metal-based catalytic systems. Due to its stability and reactivity, it is a preferred choice for researchers working on complex organic syntheses.

The compound’s unique chemical properties, including its stable structure and specific reactivity, make it a preferred choice in laboratory settings. It exhibits high catalytic efficiency and selectivity, allowing for controlled reactions under various conditions. Its ability to interact with a wide range of organic substrates enhances its versatility, making it suitable for diverse applications. Additionally, its chemical inertness under normal storage conditions ensures that it retains its catalytic activity when needed, reducing the risk of degradation or unwanted side reactions.

In Indonesian laboratories, Bis(8-quinolinolato)copper(II) is extensively used in organic chemistry research, particularly in cross-coupling reactions that require transition metal catalysts. Its reliability and effectiveness in promoting C-C bond formation make it a valuable tool for chemists working on synthetic pathways, drug development, and material science. Its widespread use highlights its importance in advancing chemical research in the region.

TCI brochures (PDF)

  • Cross-coupling reactions benefit from Bis(8-quinolinolato)copper(II) due to its ability to activate carbon-carbon bonds and promote efficient coupling under mild conditions.
  • Organic synthesis projects often utilize this compound as a transition metal catalyst to achieve high yields and selectivity in complex molecular transformations.
  • Catalytic systems in polymer chemistry rely on this material to facilitate the formation of stable carbon-carbon linkages, enhancing the structural integrity of synthetic polymers.
  • Medicinal chemistry research employs this compound to enable the synthesis of bioactive compounds that require precise C-C bond formation for functional group placement.
  • Analytical chemistry applications use it as a reagent in catalytic assays to study reaction mechanisms and evaluate the performance of transition metal catalysts.

Brand TCI
CAS number 10380-28-6
Molecular formula —
Purity —
Category Chemistry > Catalysis and Inorganic Chemistry > Cross-coupling Reaction using Transition Metal Catalysts [C-C Bond Formation]
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid powder or crystalline form, depending on packaging
Storage Store in a cool, dry place away from moisture and direct sunlight

Bis(8-quinolinolato)copper(II) should be stored in a cool, dry environment to maintain its chemical stability and catalytic activity. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air, which could lead to degradation. Suitable storage containers include glass or high-density polyethylene (HDPE) bottles that are resistant to chemical interaction. In laboratory settings, it should be handled with appropriate personal protective equipment (PPE) such as gloves and safety goggles to ensure safe handling. Avoid direct contact with skin and inhalation of dust, especially during weighing or transfer. Proper labeling and storage in a designated chemical cabinet are essential to prevent accidental exposure and ensure compliance with safety protocols.

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