Methyl5-(trifluoromethyl)pyrazine-2-carboxylate

97%

Reagent Code: #213963
fingerprint
CAS Number 1346252-26-3

science Other reagents with same CAS 1346252-26-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.12 g/mol
Formula C₇H₅F₃N₂O₂
badge Registry Numbers
MDL Number MFCD22544075
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and antiviral agents. Its structure allows for easy modification in drug design, enhancing metabolic stability and bioavailability. Commonly employed in medicinal chemistry for constructing pyrazine-based scaffolds that exhibit biological activity. Also utilized in agrochemical research for developing novel pesticides due to its electron-withdrawing trifluoromethyl group, which can improve lipophilicity and target binding.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,420.00
inventory 250mg
10-20 days ฿10,820.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Methyl5-(trifluoromethyl)pyrazine-2-carboxylate
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and antiviral agents. Its structure allows for easy modification in drug design, enhancing metabolic stability and bioavailability. Commonly employed in medicinal chemistry for constructing pyrazine-based scaffolds that exhibit biological activity. Also utilized in agrochemical research for developing novel pesticides due to its electron-withdrawing trifluoromethyl group, which can improve lipo

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and antiviral agents. Its structure allows for easy modification in drug design, enhancing metabolic stability and bioavailability. Commonly employed in medicinal chemistry for constructing pyrazine-based scaffolds that exhibit biological activity. Also utilized in agrochemical research for developing novel pesticides due to its electron-withdrawing trifluoromethyl group, which can improve lipophilicity and target binding.

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...