Methyl 2,4-dioxo-4-(2-thienyl)butanoate

97%

Reagent Code: #205243
fingerprint
CAS Number 57409-51-5

science Other reagents with same CAS 57409-51-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.23 g/mol
Formula C₉H₈O₄S
badge Registry Numbers
MDL Number MFCD01249731
inventory_2 Storage & Handling
Storage Room temperature, flammable area

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antihistamines and anti-inflammatory agents. Its structure, featuring a methyl ester, 1,3-diketo functionality, and a 2-thienyl group, allows for easy functionalization, making it valuable in constructing heterocyclic compounds. Commonly employed in research settings for developing new bioactive molecules and in the preparation of thiophene-containing organic materials. Also utilized in the design of specialty chemicals where conjugated systems enhance reactivity or optical properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿341.00
inventory 1g
10-20 days ฿1,248.50
inventory 5g
10-20 days ฿4,504.50

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Methyl 2,4-dioxo-4-(2-thienyl)butanoate
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antihistamines and anti-inflammatory agents. Its structure, featuring a methyl ester, 1,3-diketo functionality, and a 2-thienyl group, allows for easy functionalization, making it valuable in constructing heterocyclic compounds. Commonly employed in research settings for developing new bioactive molecules and in the preparation of thiophene-containing organic materials. Also utilized in the design of special

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antihistamines and anti-inflammatory agents. Its structure, featuring a methyl ester, 1,3-diketo functionality, and a 2-thienyl group, allows for easy functionalization, making it valuable in constructing heterocyclic compounds. Commonly employed in research settings for developing new bioactive molecules and in the preparation of thiophene-containing organic materials. Also utilized in the design of specialty chemicals where conjugated systems enhance reactivity or optical properties.

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...