4-(3-Pyridyl)-1-butanol

≥95%

Reagent Code: #173304
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CAS Number 60753-14-2

science Other reagents with same CAS 60753-14-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.21 g/mol
Formula C₉H₁₃NO
badge Registry Numbers
MDL Number MFCD18802565
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic receptor ligands and smoking cessation agents. It serves as a building block in the development of compounds targeting neurological disorders due to its structural similarity to nicotine. Also employed in the preparation of pyridine-containing polymers and functionalized ligands for catalysis. Its hydroxyl group allows for easy derivatization, making it valuable in medicinal chemistry for creating analogs and probing structure-activity relationships.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,160.00
inventory 250mg
10-20 days ฿2,100.00
inventory 1g
10-20 days ฿5,320.00
inventory 5g
10-20 days ฿16,840.00

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4-(3-Pyridyl)-1-butanol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic receptor ligands and smoking cessation agents. It serves as a building block in the development of compounds targeting neurological disorders due to its structural similarity to nicotine. Also employed in the preparation of pyridine-containing polymers and functionalized ligands for catalysis. Its hydroxyl group allows for easy derivatization, making it valuable in medicinal chemistry for creating

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic receptor ligands and smoking cessation agents. It serves as a building block in the development of compounds targeting neurological disorders due to its structural similarity to nicotine. Also employed in the preparation of pyridine-containing polymers and functionalized ligands for catalysis. Its hydroxyl group allows for easy derivatization, making it valuable in medicinal chemistry for creating analogs and probing structure-activity relationships.

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