(2-Methoxyethoxy)Methylphenylboronic acid

96%

Reagent Code: #213155
fingerprint
CAS Number 858126-53-1

science Other reagents with same CAS 858126-53-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.0347 g/mol
Formula C₁₀H₁₅BO₄
badge Registry Numbers
MDL Number MFCD14687277
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in organic synthesis as a boronic acid coupling partner in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its (2-methoxyethoxy)methyl group enhances solubility in polar solvents, improving reaction efficiency in aqueous or mixed solvent systems. Commonly employed in the preparation of pharmaceutical intermediates and functionalized aromatic compounds. The methoxyethoxymethyl protecting group offers stability during reactions and can be removed under mild acidic conditions when needed, allowing for selective transformations in multi-step syntheses.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿15,000.00
1g
10-20 days ฿35,000.00
(2-Methoxyethoxy)Methylphenylboronic acid
No image available

Used in organic synthesis as a boronic acid coupling partner in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its (2-methoxyethoxy)methyl group enhances solubility in polar solvents, improving reaction efficiency in aqueous or mixed solvent systems. Commonly employed in the preparation of pharmaceutical intermediates and functionalized aromatic compounds. The methoxyethoxymethyl protecting group offers stability during reactions and can be removed under mild acid

Used in organic synthesis as a boronic acid coupling partner in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its (2-methoxyethoxy)methyl group enhances solubility in polar solvents, improving reaction efficiency in aqueous or mixed solvent systems. Commonly employed in the preparation of pharmaceutical intermediates and functionalized aromatic compounds. The methoxyethoxymethyl protecting group offers stability during reactions and can be removed under mild acidic conditions when needed, allowing for selective transformations in multi-step syntheses.

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...