3-Chloro-4-(pyrrolidinyl-1-carbonyl)phenylboronic acid

≥95%

Reagent Code: #90203
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CAS Number 850589-51-4

science Other reagents with same CAS 850589-51-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.49 g/mol
Formula C₁₁H₁₃BClNO₃
badge Registry Numbers
MDL Number MFCD07363776
thermostat Physical Properties
Melting Point 152-155 °C
Boiling Point 491.2 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many bioactive compounds. Additionally, it is employed in material science for the synthesis of advanced polymers and organic electronic materials, where precise molecular architecture is crucial. Its stability and reactivity make it a valuable tool in research and industrial applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,320.00

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3-Chloro-4-(pyrrolidinyl-1-carbonyl)phenylboronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many bioactive compounds. Additionally, it is employed in material science for the synthesis

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many bioactive compounds. Additionally, it is employed in material science for the synthesis of advanced polymers and organic electronic materials, where precise molecular architecture is crucial. Its stability and reactivity make it a valuable tool in research and industrial applications.

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