Lithium diisopropylamide solution

2.0 M in THF/n-heptane ethylbenzene, MkSeal

Reagent Code: #88702
label
Alias Lithium diisopropylamide; lithium diisopropylamide, lithium diisopropylamide, lithium diisopropylamide, lithium diisopropylamide
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CAS Number 4111-54-0

science Other reagents with same CAS 4111-54-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 107.12 g/mol
Formula C₆H₁₄LiN
badge Registry Numbers
EC Number 223-893-0
MDL Number MFCD00064449
thermostat Physical Properties
Boiling Point 65℃
inventory_2 Storage & Handling
Storage 2~8 ℃

description Product Description

Used extensively as a strong, non-nucleophilic base in organic synthesis, it facilitates deprotonation reactions to generate carbanions. Commonly employed in the formation of enolates from carbonyl compounds, which are key intermediates in aldol and Claisen condensations. It is also utilized in the synthesis of pharmaceuticals, agrochemicals, and complex organic molecules. Its ability to selectively deprotonate acidic protons makes it valuable in the preparation of organometallic reagents and in asymmetric synthesis. Often chosen for its solubility in organic solvents and stability at low temperatures, ensuring controlled and efficient reactions.

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Test Parameter Specification
Concentration (Titration, sec-Butanol) 1.8-2.2
Appearance Yellow to dark brown liquid

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1L
10-20 days ฿8,620.00
inventory 100ml
10-20 days ฿1,720.00
inventory 500ml
10-20 days ฿4,520.00

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Lithium diisopropylamide solution
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Used extensively as a strong, non-nucleophilic base in organic synthesis, it facilitates deprotonation reactions to generate carbanions. Commonly employed in the formation of enolates from carbonyl compounds, which are key intermediates in aldol and Claisen condensations. It is also utilized in the synthesis of pharmaceuticals, agrochemicals, and complex organic molecules. Its ability to selectively deprotonate acidic protons makes it valuable in the preparation of organometallic reagents and in asymmetr

Used extensively as a strong, non-nucleophilic base in organic synthesis, it facilitates deprotonation reactions to generate carbanions. Commonly employed in the formation of enolates from carbonyl compounds, which are key intermediates in aldol and Claisen condensations. It is also utilized in the synthesis of pharmaceuticals, agrochemicals, and complex organic molecules. Its ability to selectively deprotonate acidic protons makes it valuable in the preparation of organometallic reagents and in asymmetric synthesis. Often chosen for its solubility in organic solvents and stability at low temperatures, ensuring controlled and efficient reactions.

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