6-(Chloromethyl)nicotinic acid

≥95%

Reagent Code: #164164
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CAS Number 148258-27-9

science Other reagents with same CAS 148258-27-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.58 g/mol
Formula C₇H₆ClNO₂
badge Registry Numbers
MDL Number MFCD20622676
thermostat Physical Properties
Boiling Point 335.4±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.396±0.06 g/cm3(Predicted)
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic acid derivatives with biological activity. Its reactive chloromethyl group allows for easy alkylation or coupling reactions, making it valuable in creating active pharmaceutical ingredients (APIs) for drugs targeting central nervous system disorders and inflammation. Commonly employed in the development of receptor agonists and antagonists due to the pyridine ring’s affinity for biological targets. Also utilized in agrochemical synthesis for building complex molecules in crop protection agents. Its versatility in organic synthesis supports applications in medicinal chemistry research and development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,330.00
inventory 250mg
10-20 days ฿18,460.00
inventory 1g
10-20 days ฿57,880.00

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6-(Chloromethyl)nicotinic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic acid derivatives with biological activity. Its reactive chloromethyl group allows for easy alkylation or coupling reactions, making it valuable in creating active pharmaceutical ingredients (APIs) for drugs targeting central nervous system disorders and inflammation. Commonly employed in the development of receptor agonists and antagonists due to the pyridine ring’s affinity for biological targets.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic acid derivatives with biological activity. Its reactive chloromethyl group allows for easy alkylation or coupling reactions, making it valuable in creating active pharmaceutical ingredients (APIs) for drugs targeting central nervous system disorders and inflammation. Commonly employed in the development of receptor agonists and antagonists due to the pyridine ring’s affinity for biological targets. Also utilized in agrochemical synthesis for building complex molecules in crop protection agents. Its versatility in organic synthesis supports applications in medicinal chemistry research and development.

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