4-Oxo-6-(Thiophen-2-Yl)-2-Thioxo-1,2,3,4-Tetrahydropyrimidine-5-Carbonitrile

98%

Reagent Code: #222335
fingerprint
CAS Number 109532-65-2

science Other reagents with same CAS 109532-65-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.29 g/mol
Formula C₉H₅N₃OS₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of biologically active heterocyclic compounds, particularly in the development of pharmaceuticals with potential antitumor, antimicrobial, and anti-inflammatory properties. Its structure supports the formation of fused pyrimidine derivatives, which are important in medicinal chemistry for designing kinase inhibitors and other drug candidates. Also employed in agrochemical research for developing novel pesticides and herbicides due to its electron-deficient scaffold that enhances binding to biological targets. Commonly utilized in organic electronics as a building block for nitrogen- and sulfur-containing semiconducting materials.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,130.00
inventory 250mg
10-20 days ฿8,540.00
inventory 1g
10-20 days ฿20,940.00
4-Oxo-6-(Thiophen-2-Yl)-2-Thioxo-1,2,3,4-Tetrahydropyrimidine-5-Carbonitrile
No image available

Used as a key intermediate in the synthesis of biologically active heterocyclic compounds, particularly in the development of pharmaceuticals with potential antitumor, antimicrobial, and anti-inflammatory properties. Its structure supports the formation of fused pyrimidine derivatives, which are important in medicinal chemistry for designing kinase inhibitors and other drug candidates. Also employed in agrochemical research for developing novel pesticides and herbicides due to its electron-deficient scaf

Used as a key intermediate in the synthesis of biologically active heterocyclic compounds, particularly in the development of pharmaceuticals with potential antitumor, antimicrobial, and anti-inflammatory properties. Its structure supports the formation of fused pyrimidine derivatives, which are important in medicinal chemistry for designing kinase inhibitors and other drug candidates. Also employed in agrochemical research for developing novel pesticides and herbicides due to its electron-deficient scaffold that enhances binding to biological targets. Commonly utilized in organic electronics as a building block for nitrogen- and sulfur-containing semiconducting materials.

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...