S-(trifluoromethyl) 4-iodobenzothioate

97%

Reagent Code: #236463
fingerprint
CAS Number 2376271-49-5

science Other reagents with same CAS 2376271-49-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.085 g/mol
Formula C₈H₄F₃IOS
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof, inert gas

description Product Description

Used primarily as a reagent in organic synthesis, particularly in trifluoromethylation reactions. It serves as a source of the trifluoromethyl group in the development of pharmaceuticals and agrochemicals, where the introduction of fluorine atoms enhances metabolic stability, lipophilicity, and bioavailability. Its iodoaryl moiety allows for further functionalization via cross-coupling reactions, making it valuable in the construction of complex fluorinated molecules. Commonly applied in medicinal chemistry for the synthesis of fluorinated analogs of biologically active compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿6,000.00
S-(trifluoromethyl) 4-iodobenzothioate
No image available

Used primarily as a reagent in organic synthesis, particularly in trifluoromethylation reactions. It serves as a source of the trifluoromethyl group in the development of pharmaceuticals and agrochemicals, where the introduction of fluorine atoms enhances metabolic stability, lipophilicity, and bioavailability. Its iodoaryl moiety allows for further functionalization via cross-coupling reactions, making it valuable in the construction of complex fluorinated molecules. Commonly applied in medicinal chemis

Used primarily as a reagent in organic synthesis, particularly in trifluoromethylation reactions. It serves as a source of the trifluoromethyl group in the development of pharmaceuticals and agrochemicals, where the introduction of fluorine atoms enhances metabolic stability, lipophilicity, and bioavailability. Its iodoaryl moiety allows for further functionalization via cross-coupling reactions, making it valuable in the construction of complex fluorinated molecules. Commonly applied in medicinal chemistry for the synthesis of fluorinated analogs of biologically active compounds.

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...