4-Ethynyl-1-propyl-1H-pyrazole

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Reagent Code: #184972
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CAS Number 1340156-26-4

science Other reagents with same CAS 1340156-26-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 134.18 g/mol
Formula C₈H₁₀N₂
badge Registry Numbers
MDL Number MFCD17281918
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of cannabinoid receptor modulators. Its alkyne functionality allows for efficient coupling reactions, such as Sonogashira or click chemistry, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and metabolic stability in target molecules. Also utilized in the preparation of analogs for biological evaluation in neuropharmacology research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,450.00
inventory 250mg
10-20 days ฿13,300.00
inventory 1g
10-20 days ฿41,890.00

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4-Ethynyl-1-propyl-1H-pyrazole
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of cannabinoid receptor modulators. Its alkyne functionality allows for efficient coupling reactions, such as Sonogashira or click chemistry, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and metabolic stability in target molecules. Also utilized in the

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of cannabinoid receptor modulators. Its alkyne functionality allows for efficient coupling reactions, such as Sonogashira or click chemistry, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and metabolic stability in target molecules. Also utilized in the preparation of analogs for biological evaluation in neuropharmacology research.

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