3-Iodothiophene-2-carboxylicacid

98%

Reagent Code: #201141
fingerprint
CAS Number 60166-84-9

science Other reagents with same CAS 60166-84-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.05 g/mol
Formula C₅H₃IO₂S
badge Registry Numbers
MDL Number MFCD05664164
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with thiophene scaffolds. Its iodo functionality allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in medicinal chemistry for building complex organic structures. Also employed in the preparation of conjugated polymers and organic semiconductors due to the electron-rich nature of the thiophene ring, contributing to materials used in organic electronics like OLEDs and OFETs.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,170.00
inventory 250mg
10-20 days ฿1,940.00
inventory 1g
10-20 days ฿4,550.00
inventory 5g
10-20 days ฿21,290.00
3-Iodothiophene-2-carboxylicacid
No image available

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with thiophene scaffolds. Its iodo functionality allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in medicinal chemistry for building complex organic structures. Also employed in the preparation of conjugated polymers and organic semiconductors due to the electron-rich nature of the thiophene ring, co

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with thiophene scaffolds. Its iodo functionality allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in medicinal chemistry for building complex organic structures. Also employed in the preparation of conjugated polymers and organic semiconductors due to the electron-rich nature of the thiophene ring, contributing to materials used in organic electronics like OLEDs and OFETs.

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...