Organolithium

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.

Isopropyllithium CAS NO 1888-75-1

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CAS No.:1888-75-1

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Content:99.90%

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2-Ethylhexyllithium CAS NO 13067-81-7

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CAS No.:13067-81-7

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[p-(Dimethylamino)Phenyl]Lithium CAS NO 13190-50-6

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CAS No.:13190-50-6

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Lithium Pivalate CAS NO 14271-99-9

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CAS No.:14271-99-9

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Lithium Phenoxide, 98 CAS NO 17634-93-4

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CAS No.:17634-93-4

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Lithium Acetylacetonate CAS NO 18115-70-3

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CAS No.:18115-70-3

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Lithium Acetylacetonate CAS NO 19185-99-0

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CAS No.:19185-99-0

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Content:99.90%

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Lithium B-Isopinocampheyl-9-Borabicyclo[3.3.1]Nonyl Hydride CAS NO 100013-07-8

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CAS No.:100013-07-8

Grade:Pharmacy Grade

Content:99.90%

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