5-Iodonicotinic acid

≥95%

Reagent Code: #200200
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CAS Number 15366-65-1

science Other reagents with same CAS 15366-65-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.01 g/mol
Formula C₆H₄INO₂
badge Registry Numbers
MDL Number MFCD07437961
thermostat Physical Properties
Boiling Point 376.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. The iodine substituent allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex molecules. Commonly employed in the development of nicotinic acid derivatives with potential medicinal properties, including enzyme inhibitors or receptor modulators. Also utilized in the preparation of radiolabeled compounds for imaging and tracer studies due to the presence of iodine. Its carboxylic acid group facilitates conjugation or salt formation, enhancing solubility or stability in formulations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,440.00
inventory 250mg
10-20 days ฿3,560.00
inventory 1g
10-20 days ฿14,000.00
inventory 5g
10-20 days ฿48,000.00

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5-Iodonicotinic acid
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. The iodine substituent allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex molecules. Commonly employed in the development of nicotinic acid derivatives with potential medicinal properties, including enzyme inhibitors or receptor modulators. Also utilized in the preparation of radiolabeled compounds for imaging and tracer studies due to the presence of iodine.

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. The iodine substituent allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex molecules. Commonly employed in the development of nicotinic acid derivatives with potential medicinal properties, including enzyme inhibitors or receptor modulators. Also utilized in the preparation of radiolabeled compounds for imaging and tracer studies due to the presence of iodine. Its carboxylic acid group facilitates conjugation or salt formation, enhancing solubility or stability in formulations.

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