2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline

97%

Reagent Code: #117766
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CAS Number 850567-56-5

science Other reagents with same CAS 850567-56-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.53 g/mol
Formula C₁₂H₁₇BClNO₂
badge Registry Numbers
MDL Number MFCD06659926
thermostat Physical Properties
Boiling Point 361.5°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This chemical is widely used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It plays a key role in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in complex organic molecules. Its boronate ester group makes it a valuable building block for creating biologically active compounds. Additionally, it is utilized in the development of materials for organic electronics, such as OLEDs, due to its ability to facilitate the synthesis of conjugated polymers. Its applications also extend to research and development in medicinal chemistry, where it aids in the discovery of new drug candidates.

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Test Parameter Specification
Appearance Off-White to Light Yellow Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿864.00
inventory 5g
10-20 days ฿9,540.00
inventory 1g
10-20 days ฿1,944.00
inventory 250mg
10-20 days ฿1,449.00

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2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
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This chemical is widely used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It plays a key role in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in complex organic molecules. Its boronate ester group makes it a valuable building block for creating biologically active compounds. Additionally, it is utilized in the development of materials for organic electronics, such as OLEDs, due to its ability

This chemical is widely used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It plays a key role in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in complex organic molecules. Its boronate ester group makes it a valuable building block for creating biologically active compounds. Additionally, it is utilized in the development of materials for organic electronics, such as OLEDs, due to its ability to facilitate the synthesis of conjugated polymers. Its applications also extend to research and development in medicinal chemistry, where it aids in the discovery of new drug candidates.

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