2-iodo-N-(3-methylbutyl)benzamide

95%

Reagent Code: #215261
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CAS Number 349145-88-6

science Other reagents with same CAS 349145-88-6

blur_circular Chemical Specifications

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Weight 317.17 g/mol
Formula C₁₂H₁₆INO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. The iodo substituent allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic structures. The amide group provides stability and can participate in hydrogen bonding, which is beneficial in drug design for enhancing target binding. Commonly employed in the development of analgesic or anti-inflammatory agents due to the structural similarity with known active molecules. Also utilized in radiolabeling studies and medicinal chemistry research for probing biological pathways.

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inventory 1g
10-20 days ฿20,700.00

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2-iodo-N-(3-methylbutyl)benzamide
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. The iodo substituent allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic structures. The amide group provides stability and can participate in hydrogen bonding, which is beneficial in drug design for enhancing target binding. Commonly employed in the development of analgesic or anti-inflammatory agents due to the structural similarity with known active

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. The iodo substituent allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic structures. The amide group provides stability and can participate in hydrogen bonding, which is beneficial in drug design for enhancing target binding. Commonly employed in the development of analgesic or anti-inflammatory agents due to the structural similarity with known active molecules. Also utilized in radiolabeling studies and medicinal chemistry research for probing biological pathways.

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