3-Methoxyphenylmagnesium bromide

2.5 M solution in 2-Methyltetrahydrofuran, MkSeal

Reagent Code: #203939
fingerprint
CAS Number 36282-40-3

science Other reagents with same CAS 36282-40-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.34 g/mol
Formula C₇H₇BrMgO
badge Registry Numbers
MDL Number MFCD00672002
thermostat Physical Properties
Boiling Point 65-67 °C
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as a versatile reagent in organic synthesis, particularly in the formation of carbon-carbon bonds. It reacts with carbonyl compounds such as aldehydes, ketones, and esters to produce secondary and tertiary alcohols bearing a methoxyphenyl group, which are useful intermediates in pharmaceutical and agrochemical synthesis. It is also employed in nucleophilic addition and substitution reactions, enabling the introduction of the 3-methoxyphenyl moiety into target molecules. Its reactivity makes it valuable in the preparation of complex organic structures, including active pharmaceutical ingredients and functional materials. Due to its sensitivity to moisture and air, it is typically handled under inert atmosphere conditions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100ml
10-20 days ฿5,800.00
inventory 500ml
10-20 days ฿21,020.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-Methoxyphenylmagnesium bromide
No image available

Used as a versatile reagent in organic synthesis, particularly in the formation of carbon-carbon bonds. It reacts with carbonyl compounds such as aldehydes, ketones, and esters to produce secondary and tertiary alcohols bearing a methoxyphenyl group, which are useful intermediates in pharmaceutical and agrochemical synthesis. It is also employed in nucleophilic addition and substitution reactions, enabling the introduction of the 3-methoxyphenyl moiety into target molecules. Its reactivity makes it valua

Used as a versatile reagent in organic synthesis, particularly in the formation of carbon-carbon bonds. It reacts with carbonyl compounds such as aldehydes, ketones, and esters to produce secondary and tertiary alcohols bearing a methoxyphenyl group, which are useful intermediates in pharmaceutical and agrochemical synthesis. It is also employed in nucleophilic addition and substitution reactions, enabling the introduction of the 3-methoxyphenyl moiety into target molecules. Its reactivity makes it valuable in the preparation of complex organic structures, including active pharmaceutical ingredients and functional materials. Due to its sensitivity to moisture and air, it is typically handled under inert atmosphere conditions.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...