4-Chloro-2-methylphenylboronic Acid (contains varying amounts of Anhydride)

98%

Reagent Code: #90626
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CAS Number 209919-30-2

science Other reagents with same CAS 209919-30-2

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scatter_plot Molecular Information
Weight 170.40 g/mol
Formula C₇H₈BClO₂
badge Registry Numbers
MDL Number MFCD02683107
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex molecules for pharmaceuticals and agrochemicals. Acts as a key intermediate in the production of active pharmaceutical ingredients (APIs) and fine chemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Commonly employed in the development of drugs targeting various diseases, including cancer and inflammation. Also utilized in material science for the synthesis of organic electronic materials and polymers.

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Test Parameter Specification
Purity 97.5-100%
Appearance White to light yellow crystalline powder

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿387.00
inventory 5g
10-20 days ฿810.00

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4-Chloro-2-methylphenylboronic Acid (contains varying amounts of Anhydride)
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex molecules for pharmaceuticals and agrochemicals. Acts as a key intermediate in the production of active pharmaceutical ingredients (APIs) and fine chemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Commonly employed in the development of drugs targeting various diseases, including cancer and inflammation. Also utilized in mat

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex molecules for pharmaceuticals and agrochemicals. Acts as a key intermediate in the production of active pharmaceutical ingredients (APIs) and fine chemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Commonly employed in the development of drugs targeting various diseases, including cancer and inflammation. Also utilized in material science for the synthesis of organic electronic materials and polymers.

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