(4-Bromobenzyl)triphenylphosphonium bromide

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Reagent Code: #68962
label
Alias (4-Bromobenzyl)triphenylphosphine bromide;
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CAS Number 51044-13-4

science Other reagents with same CAS 51044-13-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 512.22 g/mol
Formula C₂₅H₂₁Br₂P
badge Registry Numbers
MDL Number MFCD00051922
thermostat Physical Properties
Melting Point 270-273 °C
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

This compound is primarily used as a key reagent in organic synthesis, particularly in the Wittig reaction, which is a widely employed method for the formation of alkenes. It facilitates the conversion of aldehydes and ketones into alkenes by generating a phosphonium ylide intermediate. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its bromine substituent enhances its reactivity and selectivity in certain transformations, making it useful in the preparation of specific target compounds. Its application extends to materials science, where it can be used in the development of organic electronic materials and polymers.

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Test Parameter Specification
Purity 97.5-100
Appearance WHITE TO LIGHT YELLOW POWDER

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿2,420.00
inventory 100g
10-20 days ฿6,300.00
inventory 5g
10-20 days ฿640.00
inventory 500g
10-20 days ฿23,280.00

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(4-Bromobenzyl)triphenylphosphonium bromide
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This compound is primarily used as a key reagent in organic synthesis, particularly in the Wittig reaction, which is a widely employed method for the formation of alkenes. It facilitates the conversion of aldehydes and ketones into alkenes by generating a phosphonium ylide intermediate. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its bromine substituent enhances its reactivity and selectivity in certain

This compound is primarily used as a key reagent in organic synthesis, particularly in the Wittig reaction, which is a widely employed method for the formation of alkenes. It facilitates the conversion of aldehydes and ketones into alkenes by generating a phosphonium ylide intermediate. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its bromine substituent enhances its reactivity and selectivity in certain transformations, making it useful in the preparation of specific target compounds. Its application extends to materials science, where it can be used in the development of organic electronic materials and polymers.

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