Ethyl 2-iodo-4-methylthiazole-5-carboxylate

97%

Reagent Code: #180683
fingerprint
CAS Number 53137-15-8

science Other reagents with same CAS 53137-15-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.11 g/mol
Formula C₇H₈INO₂S
badge Registry Numbers
MDL Number MFCD22200768
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of fungicides and insecticides. Its structure allows for easy functionalization, making it valuable in building complex heterocyclic systems. Commonly employed in coupling reactions to introduce the thiazole moiety into larger molecules, enhancing biological activity. Also utilized in research settings for the preparation of novel bioactive compounds targeting plant protection and medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,380.00
inventory 250mg
10-20 days ฿14,260.00
inventory 1g
10-20 days ฿38,480.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 2-iodo-4-methylthiazole-5-carboxylate
No image available

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of fungicides and insecticides. Its structure allows for easy functionalization, making it valuable in building complex heterocyclic systems. Commonly employed in coupling reactions to introduce the thiazole moiety into larger molecules, enhancing biological activity. Also utilized in research settings for the preparation of novel bioactive compounds targeting plant protection and medicinal c

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of fungicides and insecticides. Its structure allows for easy functionalization, making it valuable in building complex heterocyclic systems. Commonly employed in coupling reactions to introduce the thiazole moiety into larger molecules, enhancing biological activity. Also utilized in research settings for the preparation of novel bioactive compounds targeting plant protection and medicinal chemistry.

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...