Ethyl 4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

95%

Reagent Code: #184420
fingerprint
CAS Number 38026-46-9

science Other reagents with same CAS 38026-46-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.22 g/mol
Formula C₇H₈N₂O₃S
badge Registry Numbers
MDL Number MFCD00006074
thermostat Physical Properties
Melting Point 249-255 °C
inventory_2 Storage & Handling
Density 1.4342 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of pyrimidine-based drugs with potential antiviral and anticancer activities. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building heterocyclic compounds. It is also employed in the preparation of agrochemicals and dyes due to its reactive thiocarbonyl and ester groups. Commonly utilized in research settings for constructing fused pyrimidine ring systems found in bioactive molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,000.00
inventory 250mg
10-20 days ฿19,200.00
inventory 1g
10-20 days ฿32,800.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
No image available
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of pyrimidine-based drugs with potential antiviral and anticancer activities. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building heterocyclic compounds. It is also employed in the preparation of agrochemicals and dyes due to its reactive thiocarbonyl and ester groups. Commonly utilized in research settings for constructing fused pyrimidine ring systems found in
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of pyrimidine-based drugs with potential antiviral and anticancer activities. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building heterocyclic compounds. It is also employed in the preparation of agrochemicals and dyes due to its reactive thiocarbonyl and ester groups. Commonly utilized in research settings for constructing fused pyrimidine ring systems found in bioactive molecules.
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...