(5,6,7,8-Tetrahydronaphthalen-2-yl)boronic acid

98%

Reagent Code: #244802
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CAS Number 405888-56-4

science Other reagents with same CAS 405888-56-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.02 g/mol
Formula C₁₀H₁₃BO₂
badge Registry Numbers
MDL Number MFCD11183308
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid functionality allows for mild and selective coupling with aryl or heteroaryl halides, making it valuable in the preparation of complex organic molecules, particularly in drug discovery. The tetrahydronaphthalene core provides a rigid, lipophilic structure that can enhance binding affinity in bioactive compounds. Commonly employed in the synthesis of potential therapeutic agents targeting central nervous system disorders and hormonal pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,690.00
inventory 5g
10-20 days ฿63,430.00
inventory 1g
10-20 days ฿16,370.00
inventory 10g
10-20 days ฿114,250.00
inventory 250mg
10-20 days ฿6,200.00
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(5,6,7,8-Tetrahydronaphthalen-2-yl)boronic acid
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Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid functionality allows for mild and selective coupling with aryl or heteroaryl halides, making it valuable in the preparation of complex organic molecules, particularly in drug discovery. The tetrahydronaphthalene core provides a rigid, lipophilic structure that can enhance binding affinity in bioactive comp

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid functionality allows for mild and selective coupling with aryl or heteroaryl halides, making it valuable in the preparation of complex organic molecules, particularly in drug discovery. The tetrahydronaphthalene core provides a rigid, lipophilic structure that can enhance binding affinity in bioactive compounds. Commonly employed in the synthesis of potential therapeutic agents targeting central nervous system disorders and hormonal pathways.

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