(4-Chloro-2-(pentyloxy)phenyl)boronic acid

97%

Reagent Code: #164899
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CAS Number 2096338-13-3

science Other reagents with same CAS 2096338-13-3

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It serves as a key building block in the development of pharmaceuticals and agrochemicals, as well as advanced materials such as electronic components and luminescent compounds, where the boronic acid group enables selective transformations. Its chloro and pentyloxy substituents provide sites for further functionalization, making it valuable in the design of complex aromatic compounds. Commonly applied in medicinal chemistry for constructing biaryl systems found in bioactive molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿2,930.00
1g
10-20 days ฿8,540.00
5g
10-20 days ฿29,200.00
100mg
10-20 days ฿1,730.00
(4-Chloro-2-(pentyloxy)phenyl)boronic acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It serves as a key building block in the development of pharmaceuticals and agrochemicals, as well as advanced materials such as electronic components and luminescent compounds, where the boronic acid group enables selective transformations. Its chloro and pentyloxy substituents provide sites for further functionalization, making it valuable in the design of complex aromatic compounds. Commonly

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It serves as a key building block in the development of pharmaceuticals and agrochemicals, as well as advanced materials such as electronic components and luminescent compounds, where the boronic acid group enables selective transformations. Its chloro and pentyloxy substituents provide sites for further functionalization, making it valuable in the design of complex aromatic compounds. Commonly applied in medicinal chemistry for constructing biaryl systems found in bioactive molecules.

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