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 4-[(Octadecylamino)Carbonyl]Benzoate CAS NO 84501-54-2

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CAS No.:84501-54-2

Grade:Pharmacy Grade

Content:99.90%

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Methyllithium CAS NO 917-54-4

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CAS No.:917-54-4

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Content:99.90%

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Isobutyllithium CAS NO 920-36-5

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CAS No.:920-36-5

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Content:99.90%

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1-Lithionorbornane CAS NO 930-81-4

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CAS No.:930-81-4

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Content:99.90%

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Benzyl(Tetrahydrofuran)Lithium CAS NO 93941-97-0

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CAS No.:93941-97-0

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Content:99.90%

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3-T-Butyldimethylsiloxypropyllithium CAS NO 97057-70-0

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CAS No.:97057-70-0

Grade:Pharmacy Grade

Content:99.90%

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4-(Dimethylamino)-4-Methylpent-2-Ynoic Acid Lithium Salt CAS NO 98426-27-8

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CAS No.:98426-27-8

Grade:Pharmacy Grade

Content:99.90%

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Lithium 2-(Morpholinomethyl)Benzoate, Tech CAS NO 904696-60-2

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CAS No.:904696-60-2

Grade:Pharmacy Grade

Content:99.90%

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