N,N-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-propanamine

97%

Reagent Code: #121300
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CAS Number 847818-72-8

science Other reagents with same CAS 847818-72-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.19 g/mol
Formula C₁₄H₂₆BN₃O₂
badge Registry Numbers
MDL Number MFCD11983295
thermostat Physical Properties
Boiling Point 383.9°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile building block, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, its pyrazole moiety is often leveraged in drug discovery for creating compounds with potential biological activity, such as anti-inflammatory, antimicrobial, or anticancer properties. The presence of the dimethylamine group further enhances its utility in modifying the physicochemical properties of target molecules, improving solubility or bioavailability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,961.00
inventory 1g
10-20 days ฿11,844.00
inventory 250mg
10-20 days ฿5,076.00

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N,N-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-propanamine
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This chemical is primarily utilized in organic synthesis as a versatile building block, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, its pyrazole moiety is often leveraged in drug discovery for creating compounds with potential biological activity, such as anti-inflammatory, antimicrobial, or anticancer properties. The presence of the dimethylamine group further enhances its utility in modifying the physicochemical properties of target molecules, improving solubility or bioavailability.
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