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P-Methoxyphenylmagnesium Bromide 0.5 M In Thf

P-Methoxyphenylmagnesium Bromide 0.5 M In Thf

P-Methoxyphenylmagnesium Bromide 0.5 M In Thf

P-Methoxyphenylmagnesium Bromide 0.5 M In Thf

P-Methoxyphenylmagnesium Bromide 0.5 M In Thf

P-Methoxyphenylmagnesium Bromide 0.5 M In Thf

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P-Methoxyphenylmagnesium Bromide 0.5 M In Thf

Price 2000.0 INR/ Kg

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P-Methoxyphenylmagnesium Bromide 0.5 M In Thf Specification

Place of Origin
India

Boiling point
66 C

Molecular Weight
211.34 g/mol Milligram (mg)

Melting Point
-108 C

CAS No
13139-86-1

Usage
It Is Commonly Used In Pharmaceutical, Agrochemical, And Fine Chemical Industries For The Preparation Of Alcohols, Ketones, And Complex Aromatic Intermediates Via Reactions With Aldehydes, Ketones, Esters, And Other Electrophiles. The Presence Of The Electron-Donating Methoxy Group Enhances Its Reactivity In Electrophilic Coupling Reactions. It Is Also Used In Research For Advanced Organometallic Synthesis And Aromatic Functionalization.

Purity
96-98%

Appearance
Colorless to pale yellow solution

Application
Pharmaceutical Industry

Color
Other

Form
Liquid

About P-Methoxyphenylmagnesium Bromide 0.5 M In Thf

We Are Supplier, Exporter And Contract Manufacturer.Technical Profile P-Methoxyphenylmagnesium Bromide 0.5 M In Thf, A High-Purity Raw Chemical Material Supplied By Triveni Chemicals For Industrial Manufacturing And Laboratory Synthesis.

P-Methoxyphenylmagnesium Bromide 0.5 M In Thf Is A Grignard Reagent Widely Used In Organic Synthesis As A Strong Nucleophile For CarbonCarbon Bond Formation. It Is Supplied As A 0.5 Molar Solution In Tetrahydrofuran (Thf) And Appears As A Clear To Pale Yellow Solution Under An Inert Atmosphere. The Compound Is Highly Sensitive To Moisture, Oxygen, And Carbon Dioxide, And Reacts Violently With Water, Requiring Strict Handling Under Dry Nitrogen Or Argon Conditions.

It Is Commonly Used In Pharmaceutical, Agrochemical, And Fine Chemical Industries For The Preparation Of Alcohols, Ketones, And Complex Aromatic Intermediates Via Reactions With Aldehydes, Ketones, Esters, And Other Electrophiles. The Presence Of The Electron-Donating Methoxy Group Enhances Its Reactivity In Electrophilic Coupling Reactions. It Is Also Used In Research For Advanced Organometallic Synthesis And Aromatic Functionalization. Due To Its Flammable And Highly Reactive Nature, Proper Safety Precautions And Inert Storage Conditions Are Essential.

P-Methoxyphenylmagnesium Bromide 0.5 M In Thf

P-Methoxyphenylmagnesium Bromide 0.5 M In Thf

P-Methoxyphenylmagnesium Bromide 0.5 M In Thf

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