5-Bromo-2-thiophenecarboxaldehyde

97%

Reagent Code: #142942
label
Alias 5-Bromothiophene-2-formaldehyde
fingerprint
CAS Number 4701-17-1

science Other reagents with same CAS 4701-17-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.05 g/mol
Formula C₅H₃BrOS
badge Registry Numbers
EC Number 225-176-8
MDL Number MFCD00005432
thermostat Physical Properties
Boiling Point 105-107 °C/11 mmHg(lit.)
inventory_2 Storage & Handling
Density 1.607 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active compounds. Its aldehyde and bromo functional groups allow for versatile chemical transformations, such as cross-coupling reactions and nucleophilic substitutions. Commonly employed in the preparation of thiophene-based heterocycles, which are important scaffolds in drug discovery. Also utilized in the manufacture of organic semiconductors and electronic materials due to the electron-rich nature of the thiophene ring.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿580.00
inventory 25g
10-20 days ฿1,580.00
inventory 100g
10-20 days ฿6,250.00
inventory 500g
10-20 days ฿31,230.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-Bromo-2-thiophenecarboxaldehyde
No image available

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active compounds. Its aldehyde and bromo functional groups allow for versatile chemical transformations, such as cross-coupling reactions and nucleophilic substitutions. Commonly employed in the preparation of thiophene-based heterocycles, which are important scaffolds in drug discovery. Also utilized in the manufacture of organic semiconductors and electronic materials due to

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active compounds. Its aldehyde and bromo functional groups allow for versatile chemical transformations, such as cross-coupling reactions and nucleophilic substitutions. Commonly employed in the preparation of thiophene-based heterocycles, which are important scaffolds in drug discovery. Also utilized in the manufacture of organic semiconductors and electronic materials due to the electron-rich nature of the thiophene ring.

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...