3-(Trifluoromethyl)benzenesulfonylchloride

98%

Reagent Code: #240303
fingerprint
CAS Number 777-44-6

science Other reagents with same CAS 777-44-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.62 g/mol
Formula C₇H₄ClF₃O₂S
badge Registry Numbers
MDL Number MFCD00014724
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfa drugs and other bioactive molecules. Its electrophilic sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for introducing the 3-(trifluoromethyl)phenylsulfonyl moiety into target compounds. Widely applied in medicinal chemistry for constructing sulfonamide-based inhibitors, especially in agrochemicals and antitumor agents. Also employed in materials science for modifying polymer reactivity and enhancing thermal stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿168.00
inventory 5g
10-20 days ฿460.00
inventory 25g
10-20 days ฿1,650.00
inventory 100g
10-20 days ฿6,170.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-(Trifluoromethyl)benzenesulfonylchloride
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfa drugs and other bioactive molecules. Its electrophilic sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for introducing the 3-(trifluoromethyl)phenylsulfonyl moiety into target compounds. Widely applied in medicinal chemistry for constructing sulfonamide-based inhibitors, especially in agrochemicals and antitumor agents. Also employed in materials science for modifyi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfa drugs and other bioactive molecules. Its electrophilic sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for introducing the 3-(trifluoromethyl)phenylsulfonyl moiety into target compounds. Widely applied in medicinal chemistry for constructing sulfonamide-based inhibitors, especially in agrochemicals and antitumor agents. Also employed in materials science for modifying polymer reactivity and enhancing thermal stability.

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...