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.

Organorhodium

Organorhodium compounds are renowned for their exceptional catalytic performance in asymmetric hydrogenation, hydroformylation, and carbon–carbon coupling reactions. Their ability to deliver high enantioselectivity, even under mild conditions, makes them indispensable in the synthesis of chiral pharmaceuticals, fragrances, and specialty fine chemicals. Rhodium catalysts also play a central role in industrial hydroformylation processes used to produce aldehydes and alcohols from olefins on massive commercial scales. Their efficiency, tunable ligand environments, and compatibility with diverse substrates allow precise control over stereochemistry and reaction pathways. Despite rhodium’s rarity and high cost, its unparalleled catalytic capabilities ensure continued demand across pharmaceutical, petrochemical, and advanced material industries.

Tetrakis(Acetato)Bis(Cyclopentadienyl)D& CAS NO 11077-92-2

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Chlorobis(Ethylene)Rhodium (I) Dimer CAS NO 12081-16-2

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CAS No.:12081-16-2

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Acetylacetonatobis(Ethylene)Rhodium(I) CAS NO 12082-47-2

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Di-U-Acetatobis-(1,5-Cyclooctadiene)-Dirhodium CAS NO 12097-36-8

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CAS No.:12097-36-8

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Dichlorohydrotris(Triphenylphosphine)Rhodium CAS NO 12124-48-0

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CAS No.:12124-48-0

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Methoxy(Cyclooctadiene)Rhodium(I) Dimer CAS NO 12148-72-0

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Acetylacetonato(1,5-Cyclooctadiene)Rhodium(I) CAS NO 12245-39-5

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(Bicyclo[2.2.1]Hepta-2,5-Diene)Chlororhodium(I) Dimer CAS NO 12257-42-0

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Organolithium

Organolithium compounds are among the most powerful bases and nucleophiles in synthetic chemistry, enabling rapid metalation, deprotonation, and carbon–carbon bond formation with exceptional efficiency. Their ability to react with a wide variety of electrophiles allows chemists to construct complex molecular structures and access reactive intermediates that are difficult to generate by other means. Organolithium reagents play a critical role in polymer initiation, pharmaceutical intermediate synthesis, and the preparation of advanced materials. Despite their high reactivity and sensitivity to air and moisture, they remain indispensable due to their unique selectivity and broad synthetic utility. Their rapid kinetics and predictable behavior make them essential tools for modern organic synthesis and industrial-scale processes requiring precise control over carbon framework construction.

n-Butyllithium CAS NO 109-72-8

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Dilithium Acetylide CAS NO 1070-75-3

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CAS No.:1070-75-3

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Lithium Hydrogenacetylide CAS NO 1111-64-4

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CAS No.:1111-64-4

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Benzhydrol, 4,4'-Dimethyl-, Lithium Salt (8Ci) CAS NO 1211-17-2

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CAS No.:1211-17-2

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Lithium, Ferrocenyl-(8Ci,9Ci) CAS NO 1271-15-4

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Propene-1-Ide CAS NO 1724-46-5

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CAS No.:1724-46-5

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(2-Pyridylmethyl)Lithium CAS NO 1749-29-7

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CAS No.:1749-29-7

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[(2-Aminoethyl)Amino]Lithium CAS NO 1847-46-7

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Organoruthenium

Organoruthenium compounds are highly versatile catalysts known for their exceptional performance in olefin metathesis, photoredox catalysis, hydrogenation, and C–H activation. Ruthenium-based catalysts, especially Grubbs-type complexes, revolutionized polymer chemistry and enabled efficient synthesis of complex ring structures and functional materials. Their stability, tunable ligand environments, and tolerance toward air and moisture provide significant advantages over many other transition-metal systems. Organoruthenium compounds also play critical roles in the development of pharmaceuticals, smart materials, and organic electronic components. Their ability to facilitate difficult bond transformations under mild conditions makes them essential tools for next-generation chemical innovation.

Ruthenium(Iii) Chloride CAS NO 10049-08-8

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(S,S)-n-(p-Toluenesulfonyl)-1,2-Diphenylethanediamine(Chloro)(p-Cymene)Ruthenium(Ii) CAS NO 192139-90-5

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CAS No.:192139-90-5

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Grubbs Catalyst 2Nd Generation CAS NO 246047-72-3

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CAS No.:246047-72-3

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Bis(Cyclopentadienyl)Ruthenium CAS NO 1287-13-4

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Acetylruthenocene CAS NO 1316-92-3

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Chloroborane CAS NO 10388-28-0

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Tetrakis(Dimethylsulfoxide)Dichlororuthenium (Ii) CAS NO 11070-19-2

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CAS No.:11070-19-2

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Dicarbonylcyclopentadienylruthenium(Ii) Dimer CAS NO 12132-87-5

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Organoaluminum

Organoaluminum compounds are highly reactive alkylating agents widely used in polymerization catalysis, reduction chemistry, and fine chemical synthesis. They serve as essential cocatalysts in Ziegler–Natta polymerization, enabling large-scale production of polyethylene and polypropylene with controlled molecular weight and stereochemistry. Their strong Lewis acidity allows activation of various substrates, while their ability to participate in transmetalation and hydride-transfer reactions expands their synthetic applicability. Despite requiring careful handling due to their sensitivity and pyrophoric nature, organoaluminum reagents remain indispensable in industrial chemistry. Their combination of reactivity, catalytic efficiency, and tunability makes them foundational materials in polymer science, materials engineering, and advanced organic synthesis.

Triisobutylaluminum CAS NO 100-99-2

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Tri-n-Hexyl Aluminum CAS NO 1116-73-0

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Tri-n-Propylaluminium CAS NO 102-67-0

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CAS No.:102-67-0

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Tetraethyldialuminoxane CAS NO 1069-83-6

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CAS No.:1069-83-6

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Tri-n-Octylaluminium CAS NO 1070-00-4

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Tripropyl Aluminium CAS NO 1102-67-0

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Tri-n-Butylaluminum CAS NO 1116-70-7

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Dimethylaluminum Chloride CAS NO 1184-58-3

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Organomagnesium

Organomagnesium compounds, commonly known as Grignard reagents, are foundational tools in organic synthesis due to their strong nucleophilicity and ability to form carbon–carbon bonds with high efficiency. They react readily with carbonyl compounds, epoxides, and various electrophiles, enabling rapid construction of alcohols, intermediates, and complex molecular frameworks. Grignard reagents are widely applied in pharmaceuticals, fragrances, agrochemicals, and polymer science. Their predictable reactivity and broad compatibility make them essential in multi-step synthetic sequences, despite their sensitivity to moisture and oxygen. On an industrial scale, organomagnesium compounds continue to support cost-effective and scalable production routes for fine chemicals and specialty materials, maintaining their status as indispensable reagents in modern chemistry.

Magnesium Methoxide CAS NO 109-88-6

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Isopropylmagnesium Chloride CAS NO 1068-55-9

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Bis(Cyclopentadienyl)Magnesium CAS NO 1284-72-6

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Benzylmagnesium Bromide CAS NO 1589-82-8

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CAS No.:1589-82-8

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4-Fluorobenzylmagnesium Chloride CAS NO 1643-73-8

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CAS No.:1643-73-8

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Allylmagnesium Bromide CAS NO 1730-25-2

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CAS No.:1730-25-2

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Cyclopentadienylmagnesium Chloride CAS NO 11112-17-7

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CAS No.:11112-17-7

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Mg(Ii) Porphine CAS NO 13007-95-9

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