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.

Lithium Thiophenoxide CAS NO 2973-86-6

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CAS No.:2973-86-6

Grade:Pharmacy Grade

Content:99.90%

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Gpp-Li CAS NO 21141-43-5

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CAS No.:21141-43-5

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Content:99.90%

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n-Hexyllithium CAS NO 21369-64-2

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CAS No.:21369-64-2

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Content:99.90%

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Lithium Tantalum Isopropoxide CAS NO 21864-24-4

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CAS No.:21864-24-4

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Content:99.90%

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(2,2,6,6-Tetramethyl-3,5-Heptanedionato)Lithium CAS NO 22441-13-0

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CAS No.:22441-13-0

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Content:99.90%

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Lithium 2-Hydroxyethoxide CAS NO 23248-23-9

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CAS No.:23248-23-9

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Content:99.90%

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Cyclopentyllithium CAS NO 23473-12-3

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CAS No.:23473-12-3

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Content:99.90%

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Ethen-1-Ide CAS NO 25012-81-1

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CAS No.:25012-81-1

Grade:Pharmacy Grade

Content:99.90%

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