2-Cyclopropyl-5-(3-methyl-1H-pyrazol-1-yl)phenylboronic acid

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Reagent Code: #89726
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CAS Number 2225178-80-1

science Other reagents with same CAS 2225178-80-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.0814 g/mol
Formula C₁₃H₁₅BN₂O₂
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This chemical, 2-Cyclopropyl-5-(3-methyl-1H-pyrazol-1-yl)phenylboronic acid, is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. The unique structure featuring a cyclopropyl group at the 2-position and a 3-methyl-1H-pyrazol-1-yl substituent at the 5-position enhances molecular diversity, making it a key intermediate for constructing complex organic molecules in the pharmaceutical industry. It aids in the development of drug candidates, including anti-cancer and anti-viral agents, by enabling efficient coupling of its boronic acid group with various aryl halides to form carbon-carbon bonds. Additionally, it finds use in material science for synthesizing advanced polymers and functional materials. Its stability and reactivity make it a versatile reagent in research and industrial applications.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿10,080.00
inventory 25mg
10-20 days ฿29,304.00
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2-Cyclopropyl-5-(3-methyl-1H-pyrazol-1-yl)phenylboronic acid
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This chemical, 2-Cyclopropyl-5-(3-methyl-1H-pyrazol-1-yl)phenylboronic acid, is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. The unique structure featuring a cyclopropyl group at the 2-position and a 3-methyl-1H-pyrazol-1-yl substituent at the 5-position enhances molecular diversity, making it a key intermediate for constructing complex organic molecules in the pharmaceutical industry. It aids in the development of drug candidates,

This chemical, 2-Cyclopropyl-5-(3-methyl-1H-pyrazol-1-yl)phenylboronic acid, is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. The unique structure featuring a cyclopropyl group at the 2-position and a 3-methyl-1H-pyrazol-1-yl substituent at the 5-position enhances molecular diversity, making it a key intermediate for constructing complex organic molecules in the pharmaceutical industry. It aids in the development of drug candidates, including anti-cancer and anti-viral agents, by enabling efficient coupling of its boronic acid group with various aryl halides to form carbon-carbon bonds. Additionally, it finds use in material science for synthesizing advanced polymers and functional materials. Its stability and reactivity make it a versatile reagent in research and industrial applications.

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