o-Tolylmagnesium bromide solution

1.0 M solution in THF, MkSeal

Reagent Code: #238856
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CAS Number 932-31-0

science Other reagents with same CAS 932-31-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.34 g/mol
Formula C₇H₇BrMg
badge Registry Numbers
EC Number 213-250-2
MDL Number MFCD00010350
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a versatile reagent in organic synthesis, particularly in carbon-carbon bond-forming reactions. It acts as a nucleophile in Grignard reactions, enabling the addition to carbonyl groups such as aldehydes, ketones, and esters to produce secondary and tertiary alcohols. Commonly employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where an ortho-substituted phenyl group is required. Its solution form allows for precise handling and dosing in industrial and laboratory settings, improving reaction reproducibility and safety. Also utilized in the preparation of ligands for catalysis and in the construction of complex aromatic systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100ml
10-20 days ฿2,980.00
inventory 500ml
10-20 days ฿7,350.00
o-Tolylmagnesium bromide solution
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Used as a versatile reagent in organic synthesis, particularly in carbon-carbon bond-forming reactions. It acts as a nucleophile in Grignard reactions, enabling the addition to carbonyl groups such as aldehydes, ketones, and esters to produce secondary and tertiary alcohols. Commonly employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where an ortho-substituted phenyl group is required. Its solution form allows for precise handling and dosing in industrial and laboratory setti

Used as a versatile reagent in organic synthesis, particularly in carbon-carbon bond-forming reactions. It acts as a nucleophile in Grignard reactions, enabling the addition to carbonyl groups such as aldehydes, ketones, and esters to produce secondary and tertiary alcohols. Commonly employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where an ortho-substituted phenyl group is required. Its solution form allows for precise handling and dosing in industrial and laboratory settings, improving reaction reproducibility and safety. Also utilized in the preparation of ligands for catalysis and in the construction of complex aromatic systems.

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