6-Iodo-2-(methylthio)benzo[d]thiazole

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Reagent Code: #200679
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CAS Number 1161730-21-7

science Other reagents with same CAS 1161730-21-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 307.17 g/mol
Formula C₈H₆INS₂
badge Registry Numbers
MDL Number MFCD20482768
thermostat Physical Properties
Boiling Point 381.0±34.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.95±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antithyroid agents and kinase inhibitors. Its structure supports the formation of biologically active molecules by enabling cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aromatic or heteroaromatic moieties. Also employed in the preparation of radiolabeled compounds for imaging studies due to the presence of iodine. Additionally, it serves as a building block in agrochemicals for designing novel pesticides with improved efficacy.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,950.00
inventory 250mg
10-20 days ฿8,410.00
inventory 1g
10-20 days ฿22,700.00

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6-Iodo-2-(methylthio)benzo[d]thiazole
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antithyroid agents and kinase inhibitors. Its structure supports the formation of biologically active molecules by enabling cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aromatic or heteroaromatic moieties. Also employed in the preparation of radiolabeled compounds for imaging studies due to the presence of iodine. Additionally, it serves as a building block in agrochemicals for d

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antithyroid agents and kinase inhibitors. Its structure supports the formation of biologically active molecules by enabling cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aromatic or heteroaromatic moieties. Also employed in the preparation of radiolabeled compounds for imaging studies due to the presence of iodine. Additionally, it serves as a building block in agrochemicals for designing novel pesticides with improved efficacy.

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