3,5-dichloro-4-methoxyphenylboronic acid

≥95%

Reagent Code: #170090
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CAS Number 175883-61-1

science Other reagents with same CAS 175883-61-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.85 g/mol
Formula C₇H₇BCl₂O₃
badge Registry Numbers
MDL Number MFCD04039018
inventory_2 Storage & Handling
Density 1.45±0.1 g/cm3(Predicted)
Storage 2~8℃

description Product Description

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the development of complex aromatic compounds. The presence of chlorine and methoxy substituents provides electronic and steric properties that influence reactivity and selectivity in synthesis. Commonly employed in the preparation of bioactive molecules and functional materials requiring specific substitution patterns on aromatic rings.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,900.00
inventory 5g
10-20 days ฿28,200.00
inventory 10g
10-20 days ฿49,020.00
inventory 1g
10-20 days ฿7,740.00

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3,5-dichloro-4-methoxyphenylboronic acid
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Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the development of complex aromatic compounds. The presence of chlorine and methoxy substituents provides electronic and steric properties that influence reactivity and selectivity in synthesis. Commonly employed in the preparation of bioactive mol

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the development of complex aromatic compounds. The presence of chlorine and methoxy substituents provides electronic and steric properties that influence reactivity and selectivity in synthesis. Commonly employed in the preparation of bioactive molecules and functional materials requiring specific substitution patterns on aromatic rings.

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