Phenylmagnesium chloride (27% in tetrahydrofuran, ca. 2mol/L)

2.0 M in THF, MkSeal

Reagent Code: #88918
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Alias Phenyl magnesium chloride
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CAS Number 100-59-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 136.86 g/mol
Formula C₆H₅ClMg
badge Registry Numbers
MDL Number MFCD00000464
thermostat Physical Properties
Melting Point 89-90℃
Boiling Point 230℃ (8 Torr)
inventory_2 Storage & Handling
Density 0.98 g/mL at 20 °C
Storage 2~8 ℃

description Product Description

Phenylmagnesium chloride is widely used as a Grignard reagent in organic synthesis. It is particularly valuable for forming carbon-carbon bonds, making it essential in the production of complex organic molecules. One of its primary applications is in the synthesis of alcohols through the reaction with carbonyl compounds such as aldehydes and ketones. It is also employed in the preparation of pharmaceuticals, agrochemicals, and fine chemicals, where it serves as a key intermediate. Additionally, it is used in the synthesis of biphenyl compounds and other aromatic derivatives. Its reactivity with various electrophiles makes it a versatile tool in constructing diverse organic structures.

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Test Parameter Specification
Concentration of sec-Butanol (Method) 1.8-2.2 M
Appearance Black liquid

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1L
10-20 days ฿8,980.00
inventory 100ml
10-20 days ฿2,020.00
inventory 500ml
10-20 days ฿5,200.00
inventory 800ml
10-20 days ฿8,290.00
Phenylmagnesium chloride (27% in tetrahydrofuran, ca. 2mol/L)
Phenylmagnesium chloride is widely used as a Grignard reagent in organic synthesis. It is particularly valuable for forming carbon-carbon bonds, making it essential in the production of complex organic molecules. One of its primary applications is in the synthesis of alcohols through the reaction with carbonyl compounds such as aldehydes and ketones. It is also employed in the preparation of pharmaceuticals, agrochemicals, and fine chemicals, where it serves as a key intermediate. Additionally, it is used in the synthesis of biphenyl compounds and other aromatic derivatives. Its reactivity with various electrophiles makes it a versatile tool in constructing diverse organic structures.
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