(1-(Difluoromethyl)-1H-pyrazol-4-yl)boronicacid

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Reagent Code: #179862
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CAS Number 1312693-57-4

science Other reagents with same CAS 1312693-57-4

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scatter_plot Molecular Information
Weight 161.9 g/mol
Formula C₄H₅BF₂N₂O₂
badge Registry Numbers
MDL Number MFCD21363058
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fungicides and agrochemicals. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, allowing for efficient construction of complex molecules in medicinal chemistry. Commonly employed in the preparation of bioactive compounds targeting plant pathogens, especially in crop protection agents. Also utilized in research settings for the development of new heterocyclic systems with potential biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,820.00
inventory 250mg
10-20 days ฿9,820.00
inventory 1g
10-20 days ฿26,270.00
inventory 5g
10-20 days ฿86,480.00

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(1-(Difluoromethyl)-1H-pyrazol-4-yl)boronicacid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fungicides and agrochemicals. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, allowing for efficient construction of complex molecules in medicinal chemistry. Commonly employed in the preparation of bioactive compounds targeting plant pathogens, especially in crop protection agents. Also utilized in research settings for the development of new heterocyclic systems with potential biologi
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fungicides and agrochemicals. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, allowing for efficient construction of complex molecules in medicinal chemistry. Commonly employed in the preparation of bioactive compounds targeting plant pathogens, especially in crop protection agents. Also utilized in research settings for the development of new heterocyclic systems with potential biological activity.
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