5-bromothiophene-3-carboxylic acid

97%

Reagent Code: #143588
fingerprint
CAS Number 100523-84-0

science Other reagents with same CAS 100523-84-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.05 g/mol
Formula C₅H₃BrO₂S
badge Registry Numbers
MDL Number MFCD08695074
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 thiophene-based bioactive molecules. Its bromine functionality allows for cross-coupling reactions, enabling the construction of complex organic structures. Commonly employed in the preparation of conjugated polymers and organic semiconductors due to the electron-rich nature of the thiophene ring. Also utilized in research for fabricating sensors and optoelectronic materials where functionalized thiophenes enhance performance and stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿470.00
inventory 5g
10-20 days ฿1,780.00
inventory 25g
10-20 days ฿7,390.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-bromothiophene-3-carboxylic acid
No image available

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its bromine functionality allows for cross-coupling reactions, enabling the construction of complex organic structures. Commonly employed in the preparation of conjugated polymers and organic semiconductors due to the electron-rich nature of the thiophene ring. Also utilized in research for fabricating sensors and optoelectronic materials where function

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its bromine functionality allows for cross-coupling reactions, enabling the construction of complex organic structures. Commonly employed in the preparation of conjugated polymers and organic semiconductors due to the electron-rich nature of the thiophene ring. Also utilized in research for fabricating sensors and optoelectronic materials where functionalized thiophenes enhance performance and stability.

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...