N-(5-Iodo-pyridin-2-YL)-4-methyl-benzosulfonamide

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Reagent Code: #219164
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CAS Number 209971-43-7

science Other reagents with same CAS 209971-43-7

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Weight 374.20 g/mol
Formula C₁₂H₁₁IN₂O₂S
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MDL Number MFCD09746246
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Storage Room temperature

description Product Description

Used in organic synthesis as an intermediate for pharmaceutical compounds, particularly in the development of kinase inhibitors. Exhibits utility in medicinal chemistry for constructing bioactive molecules due to the presence of reactive iodine and sulfonamide functional groups. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds in drug discovery pathways. Also serves as a building block in the preparation of heterocyclic compounds with potential antitumor and anti-inflammatory activities.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,140.00
inventory 250mg
10-20 days ฿11,410.00
inventory 1g
10-20 days ฿22,810.00

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N-(5-Iodo-pyridin-2-YL)-4-methyl-benzosulfonamide
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Used in organic synthesis as an intermediate for pharmaceutical compounds, particularly in the development of kinase inhibitors. Exhibits utility in medicinal chemistry for constructing bioactive molecules due to the presence of reactive iodine and sulfonamide functional groups. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds in drug discovery pathways. Also serves as a building block in the preparation of heterocyclic compounds with potential an

Used in organic synthesis as an intermediate for pharmaceutical compounds, particularly in the development of kinase inhibitors. Exhibits utility in medicinal chemistry for constructing bioactive molecules due to the presence of reactive iodine and sulfonamide functional groups. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds in drug discovery pathways. Also serves as a building block in the preparation of heterocyclic compounds with potential antitumor and anti-inflammatory activities.

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