3-Iodobenzo[b]thiophene

95%

Reagent Code: #200476
fingerprint
CAS Number 36748-88-6

science Other reagents with same CAS 36748-88-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.09 g/mol
Formula C₈H₅IS
badge Registry Numbers
MDL Number MFCD00176396
inventory_2 Storage & Handling
Storage 2-8°C, avoid light, inert gas storage

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the preparation of bioactive molecules due to the presence of both iodine and heterocyclic thiophene ring, enabling cross-coupling reactions like Suzuki or Heck reactions. Applied in the development of functional materials, including organic semiconductors and electronic devices, where aryl iodides act as precursors for conjugated systems. Also explored in medicinal chemistry for radiolabeling studies owing to the iodine atom, which can be replaced with radioactive isotopes for imaging or therapeutic purposes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,360.00
inventory 5g
10-20 days ฿4,600.00
inventory 10g
10-20 days ฿8,860.00
3-Iodobenzo[b]thiophene
No image available

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the preparation of bioactive molecules due to the presence of both iodine and heterocyclic thiophene ring, enabling cross-coupling reactions like Suzuki or Heck reactions. Applied in the development of functional materials, including organic semiconductors and electronic devices, where aryl iodides act as precursors for conjugated systems. Also explored in medicinal chemistry for radiolabelin

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the preparation of bioactive molecules due to the presence of both iodine and heterocyclic thiophene ring, enabling cross-coupling reactions like Suzuki or Heck reactions. Applied in the development of functional materials, including organic semiconductors and electronic devices, where aryl iodides act as precursors for conjugated systems. Also explored in medicinal chemistry for radiolabeling studies owing to the iodine atom, which can be replaced with radioactive isotopes for imaging or therapeutic purposes.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...