Ethyl 2,5-dibromothiazole-4-carboxylate

97%

Reagent Code: #181942
fingerprint
CAS Number 208264-60-2

science Other reagents with same CAS 208264-60-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 314.98 g/mol
Formula C₆H₅Br₂NO₂S
badge Registry Numbers
MDL Number MFCD09265487
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial or antifungal properties. Its structure allows for further functionalization, making it valuable in medicinal chemistry for building thiazole-based compounds. Also employed in research settings to prepare fluorescent probes and dyes due to the thiazole ring’s electronic properties. Commonly utilized in coupling reactions to form more complex heterocyclic systems in drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,620.00
inventory 5g
10-20 days ฿7,790.00
inventory 25g
10-20 days ฿33,750.00
$product.analytical_desc - NULL

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 2,5-dibromothiazole-4-carboxylate
No image available

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial or antifungal properties. Its structure allows for further functionalization, making it valuable in medicinal chemistry for building thiazole-based compounds. Also employed in research settings to prepare fluorescent probes and dyes due to the thiazole ring’s electronic properties. Commonly utilized in coupling reactions to form more complex heterocyclic

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial or antifungal properties. Its structure allows for further functionalization, making it valuable in medicinal chemistry for building thiazole-based compounds. Also employed in research settings to prepare fluorescent probes and dyes due to the thiazole ring’s electronic properties. Commonly utilized in coupling reactions to form more complex heterocyclic systems in drug discovery.

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...