Lithium 2,2,6,6-tetramethylpiperidide

97%

Reagent Code: #78409
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CAS Number 38227-87-1

science Other reagents with same CAS 38227-87-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.19 g/mol
Formula C₉H₁₈LiN
badge Registry Numbers
MDL Number MFCD00015910
inventory_2 Storage & Handling
Storage room temperature, dry, inert gas

description Product Description

Used as a strong, non-nucleophilic base in organic synthesis, particularly for deprotonating weakly acidic substrates. It is highly effective in generating carbanions, which are intermediates in various reactions like alkylations, acylations, and condensations. Commonly employed in the preparation of organolithium compounds and in the synthesis of complex molecules, including pharmaceuticals and fine chemicals. Its sterically hindered structure minimizes side reactions, making it a valuable reagent in selective transformations.

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Test Parameter Specification
Titration (Sec-Butanol) 96.5-103.5
Appearance Faint yellow to dark yellow and faint brown to dark brown; powder or solid or chunks

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿7,300.00
inventory 10g
10-20 days ฿14,120.00
inventory 1g
10-20 days ฿1,820.00

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Lithium 2,2,6,6-tetramethylpiperidide
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Used as a strong, non-nucleophilic base in organic synthesis, particularly for deprotonating weakly acidic substrates. It is highly effective in generating carbanions, which are intermediates in various reactions like alkylations, acylations, and condensations. Commonly employed in the preparation of organolithium compounds and in the synthesis of complex molecules, including pharmaceuticals and fine chemicals. Its sterically hindered structure minimizes side reactions, making it a valuable reagent in se

Used as a strong, non-nucleophilic base in organic synthesis, particularly for deprotonating weakly acidic substrates. It is highly effective in generating carbanions, which are intermediates in various reactions like alkylations, acylations, and condensations. Commonly employed in the preparation of organolithium compounds and in the synthesis of complex molecules, including pharmaceuticals and fine chemicals. Its sterically hindered structure minimizes side reactions, making it a valuable reagent in selective transformations.

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