tert-Butyl (4-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate

98%

Reagent Code: #113295
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CAS Number 1080573-28-9

science Other reagents with same CAS 1080573-28-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 353.65 g/mol
Formula C₁₇H₂₅BClNO₄
badge Registry Numbers
MDL Number MFCD23379564
thermostat Physical Properties
Boiling Point 410.4±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.14±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This reaction is crucial in creating complex organic molecules, including active pharmaceutical ingredients (APIs) and biologically active compounds. Additionally, the carbamate group provides stability and can act as a protective group for amines during synthetic processes, enabling selective reactions in multi-step syntheses. Its applications are particularly significant in the production of targeted drugs and advanced materials.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,515.00
inventory 100mg
10-20 days ฿1,647.00
inventory 250mg
10-20 days ฿2,790.00

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tert-Butyl (4-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate
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This chemical is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This reaction is crucial in creating complex organic molecules, including active pharmaceutical ingredients (APIs) and biologically active compounds. Additionally, the carbamate group provides stability and can act as a p

This chemical is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This reaction is crucial in creating complex organic molecules, including active pharmaceutical ingredients (APIs) and biologically active compounds. Additionally, the carbamate group provides stability and can act as a protective group for amines during synthetic processes, enabling selective reactions in multi-step syntheses. Its applications are particularly significant in the production of targeted drugs and advanced materials.

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