4-Isoquinolineboronic acid hydrochloride

98%

Reagent Code: #90576
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Alias 4-Isoquinoline borate hydrochloride
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CAS Number 677702-23-7

science Other reagents with same CAS 677702-23-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.44 g/mol
Formula C₉H₈BNO₂HCl
badge Registry Numbers
MDL Number MFCD05664061
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl structures. It serves as a key intermediate in pharmaceutical research, aiding in the development of new drugs. Also employed in material science for constructing advanced organic frameworks and polymers. Its boronic acid group enables selective binding to diols, making it useful in biochemical assays and sensor development. Additionally, it plays a role in catalysis and the study of enzyme inhibition mechanisms.

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Test Parameter Specification
Purity 97.5-100%
Appearance White to off-white powder or crystals
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿690.00
inventory 25g
10-20 days ฿19,600.00
inventory 1g
10-20 days ฿1,350.00
inventory 5g
10-20 days ฿5,400.00

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4-Isoquinolineboronic acid hydrochloride
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Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl structures. It serves as a key intermediate in pharmaceutical research, aiding in the development of new drugs. Also employed in material science for constructing advanced organic frameworks and polymers. Its boronic acid group enables selective binding to diols, making it useful in biochemical assays and sensor development. Additionally, it plays a role in catalysis and the study of e

Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl structures. It serves as a key intermediate in pharmaceutical research, aiding in the development of new drugs. Also employed in material science for constructing advanced organic frameworks and polymers. Its boronic acid group enables selective binding to diols, making it useful in biochemical assays and sensor development. Additionally, it plays a role in catalysis and the study of enzyme inhibition mechanisms.

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