Organometallic Compounds

Organometallic Compounds

Organometallic compounds contain metal–carbon bonds and serve as catalysts, reagents, and intermediates in pharmaceutical synthesis, polymerization reactions, and fine-chemical production. They exhibit strong catalytic activity and high selectivity, enabling transformations such as coupling, reduction, and C–C bond formation.

Organocopper

Organocopper compounds are highly versatile reagents widely used in conjugate addition, substitution, coupling, and carbon–carbon bond formation. Their ability to participate in both ionic and radical pathways gives them flexible reactivity that complements lithium, magnesium, and palladium systems. Organocopper reagents are essential in the synthesis of pharmaceuticals, natural products, and fine chemicals, enabling precise functionalization of aromatic and aliphatic substrates. They are particularly valued for forming carbon–carbon bonds with high regioselectivity and for enabling transformations that proceed under relatively mild conditions. Copper’s low cost and favorable environmental profile further support its use in large-scale industrial processes. With the growing emphasis on sustainable catalysis, organocopper chemistry continues to expand into new applications in materials, catalysis, and green synthesis.

Copper(Ii) Methoxide 97 CAS NO 1184-54-9

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CAS No.:1184-54-9

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Copper(I) Acetylide CAS NO 1117-94-8

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CAS No.:1117-94-8

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Methylcopper(I) CAS NO 1184-53-8

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CAS No.:1184-53-8

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Thiophenol Copper(I) Salt CAS NO 1192-40-1

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CAS No.:1192-40-1

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Copper Tetrammine Dichloride CAS NO 10534-87-9

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CAS No.:10534-87-9

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Diethylenetriamine-Pentaacetic Acid Cu(I CAS NO 12189-76-3

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CAS No.:12189-76-3

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Cyclopentadienyl(Triethylphosphine)Copper (I) CAS NO 12261-30-2

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CAS No.:12261-30-2

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3-Acetyl-5-sec-Butyl-4-Hydroxy-3-Pyrrolin-2-One Copper Salt CAS NO 12427-40-6

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Organotin

Organotin compounds play important roles in Stille coupling, polymer stabilization, catalytic processes, and specialized industrial applications. Their strong carbon–tin bonds and predictable reactivity allow efficient cross-coupling and functional-group transformations. Organotin reagents have been widely used in the synthesis of pharmaceuticals, electronic materials, and complex organic molecules. Certain organotin compounds also serve as stabilizers in PVC production, improving thermal resistance and material performance. However, environmental and toxicity concerns have encouraged more controlled use and strict regulation of organotin species, particularly in large-scale or consumer-facing applications. Despite these limitations, organotin chemistry remains valuable in research settings and specialized industrial processes where alternative reagents cannot match their unique reactivity.

Trimethyltin Chloride CAS NO 1066-45-1

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CAS No.:1066-45-1

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Trimethyltin Hydroxide CAS NO 56-24-6

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CAS No.:56-24-6

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Bis(Tributyltin) Oxide CAS NO 56-35-9

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CAS No.:56-35-9

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Chlorotriphenyltin CAS NO 639-58-7

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CAS No.:639-58-7

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Tributyltin Hydride CAS NO 688-73-3

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CAS No.:688-73-3

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Divinyltin Dichloride CAS NO 7532-85-6

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CAS No.:7532-85-6

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Dimethyldi(Butylthio) Tin(Iv) CAS NO 1000-40-4

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CAS No.:1000-40-4

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Di-n-Butyltin CAS NO 1002-53-5

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CAS No.:1002-53-5

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Organozinc

Organozinc compounds are prized for their mild reactivity, excellent functional-group tolerance, and compatibility with delicate molecular architectures. They play key roles in Negishi coupling and other cross-coupling reactions that proceed with high selectivity and minimal byproduct formation. Unlike more reactive organometallic reagents, organozinc species allow controlled transformations without excessive side reactions, making them ideal for complex pharmaceutical and agrochemical intermediates. Their ability to participate in nucleophilic addition, transmetalation, and radical processes enhances their synthetic versatility. Organozinc reagents also support catalytic systems involving nickel and palladium, providing clean reaction pathways. As demand for precise and sustainable chemical synthesis grows, organozinc chemistry continues to expand its relevance across fine chemical, medicinal, and material science applications.

Diphenylzinc CAS NO 1078-58-6

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Di-n-Butyl Zinc CAS NO 1119-90-0

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CAS No.:1119-90-0

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Zinc Methanolate CAS NO 1184-55-0

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CAS No.:1184-55-0

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Bis(Pentafluorophenyl)Zinc 97 CAS NO 1799-90-2

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CAS No.:1799-90-2

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Diallylzinc CAS NO 1802-55-7

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CAS No.:1802-55-7

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Zinc I-Propoxide, 99% CAS NO 13282-39-8

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CAS No.:13282-39-8

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Zinc Pentamethylenedithiocarbamate CAS NO 13878-54-1

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CAS No.:13878-54-1

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Bis(8-Quinolinolato) Zinc CAS NO 13978-85-3

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Organoiridium

Organoiridium compounds are renowned for their exceptional catalytic performance in hydrogenation, C–H activation, transfer hydrogenation, and photoredox chemistry. Their unique electronic structure enables highly selective bond transformations that are difficult to achieve with other metals. Iridium complexes are widely used in the synthesis of pharmaceuticals, fine chemicals, and chiral intermediates, often delivering outstanding enantioselectivity under mild reaction conditions. Additionally, organoiridium compounds play vital roles in optoelectronics, including phosphorescent OLED emitters used in high-resolution displays. Although iridium is one of the rarest and most expensive metals, its unparalleled catalytic efficiency continues to justify its use in transformative chemical processes. As research expands, organoiridium chemistry remains central to next-generation catalysis and advanced material development.

Dodecacarbonyltetrairidium CAS NO 11065-24-0

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CAS No.:11065-24-0

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Chloro(1,5-Cyclooctadiene)Iridium(I) Dimer CAS NO 12112-67-3

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Di-Mu-Methoxobis(1,5-Cyclooctadiene)Diiridium(I) CAS NO 12148-71-9

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Iridium I Pentanedionate-Cyclo-Octadiene Complex CAS NO 12154-84-6

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Bis(Cyclooctene)Iridium(I) Chloride, Dimer CAS NO 12246-51-4

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CAS No.:12246-51-4

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(Pentamethylcyclopentadienyl)Iridium(Iii) Chloride Dimer CAS NO 12354-84-6

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CAS No.:12354-84-6

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Iridium(Iii) Chloride Trihydrate CAS NO 13569-57-8

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(Acetylacetonato)Dicarbonyliridium(I) CAS NO 14023-80-4

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Organogermanium

Organogermanium compounds possess unique electronic properties and structural characteristics that make them attractive for use in semiconductor materials, optical technologies, and medicinal chemistry. Their ability to stabilize unusual bonding environments allows chemists to explore reactivity patterns not accessible with carbon or silicon analogues. Organogermanium species participate in hydride transfer, cycloaddition, and radical processes, offering valuable tools for synthetic innovation. In materials science, germanium-containing organometallics contribute to the development of high-performance polymers, infrared optical components, and electronic devices. Certain organogermanium compounds have also been investigated for potential biological activity, although applications remain specialized. As interest grows in novel main-group chemistry, organogermanium continues to expand its role in advanced synthesis and functional material design.

Carboxyethylgermanium Sesquioxide CAS NO 12758-40-6

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6-Germaspiro[5.5]Undecane CAS NO 180-98-3

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CAS No.:180-98-3

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Tetraphenylgermane CAS NO 1048-05-1

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CAS No.:1048-05-1

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Trimethylgermanium Bromide CAS NO 1066-37-1

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CAS No.:1066-37-1

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Trimethylgermanium Iodide CAS NO 1066-38-2

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CAS No.:1066-38-2

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Bromotriethylgermane CAS NO 1067-10-3

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CAS No.:1067-10-3

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Tetra-n-Butylgermane CAS NO 1067-42-1

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CAS No.:1067-42-1

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Phenyltrichlorogermane CAS NO 1074-29-9

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