Lithium tert-butoxide

99%

Reagent Code: #88729
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Alias Lithium tert-butoxide
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CAS Number 1907-33-1
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Properties Easy to absorb moisture

science Other reagents with same CAS 1907-33-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 80.05 g/mol
Formula C₄H₉LiO
badge Registry Numbers
EC Number 217-611-5
MDL Number MFCD00050479
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Lithium tert-butoxide is widely used as a strong base in organic synthesis, particularly in deprotonation reactions. It is highly effective in generating carbanions from weakly acidic compounds, making it valuable in the formation of carbon-carbon bonds. This chemical is commonly employed in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. Additionally, it serves as a catalyst or reagent in various polymerization processes, aiding in the production of specialized polymers. Its sterically hindered nature also makes it useful in selective reactions where less bulky bases might lead to unwanted side products.

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Test Parameter Specification
CA 0-0.01
Li2CO3 LiOH (LiOH) 0-0.8
Iron (Fe) 0-0.001%
PB 0-0.005
Purity 98.5-101.5%
Appearance White or light yellow powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 2.5kg
10-20 days ฿47,510.00
inventory 25g
10-20 days ฿760.00
inventory 100g
10-20 days ฿2,690.00
inventory 500g
10-20 days ฿11,600.00

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Lithium tert-butoxide
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Lithium tert-butoxide is widely used as a strong base in organic synthesis, particularly in deprotonation reactions. It is highly effective in generating carbanions from weakly acidic compounds, making it valuable in the formation of carbon-carbon bonds. This chemical is commonly employed in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. Additionally, it serves as a catalyst or reagent in various polymerization processes, aiding in the production of specialized

Lithium tert-butoxide is widely used as a strong base in organic synthesis, particularly in deprotonation reactions. It is highly effective in generating carbanions from weakly acidic compounds, making it valuable in the formation of carbon-carbon bonds. This chemical is commonly employed in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. Additionally, it serves as a catalyst or reagent in various polymerization processes, aiding in the production of specialized polymers. Its sterically hindered nature also makes it useful in selective reactions where less bulky bases might lead to unwanted side products.

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