4-Bromo-3-fluorobenzenesulfonyl Chloride

98%

Reagent Code: #144752
fingerprint
CAS Number 351003-51-5

science Other reagents with same CAS 351003-51-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.50 g/mol
Formula C₆H₃BrClFO₂S
badge Registry Numbers
MDL Number MFCD03094150
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of sulfonamide-based compounds. Its reactive sulfonyl chloride group allows for easy attachment to amines or alcohols, forming sulfonamides or sulfonate esters, which are key structures in many bioactive molecules. The bromine at the 4-position and fluorine at the 3-position on the benzene ring enhance solubility and binding affinity to biological targets, making it valuable in creating potent drug candidates. Commonly employed in medicinal chemistry for constructing enzyme inhibitors and receptor ligands. Also utilized in the preparation of functionalized aromatic compounds for research in organic synthesis and drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿156.00
inventory 5g
10-20 days ฿780.00
inventory 25g
10-20 days ฿3,510.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Bromo-3-fluorobenzenesulfonyl Chloride
No image available

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of sulfonamide-based compounds. Its reactive sulfonyl chloride group allows for easy attachment to amines or alcohols, forming sulfonamides or sulfonate esters, which are key structures in many bioactive molecules. The bromine at the 4-position and fluorine at the 3-position on the benzene ring enhance solubility and binding affinity to biological targets, making it valuable in creating potent d

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of sulfonamide-based compounds. Its reactive sulfonyl chloride group allows for easy attachment to amines or alcohols, forming sulfonamides or sulfonate esters, which are key structures in many bioactive molecules. The bromine at the 4-position and fluorine at the 3-position on the benzene ring enhance solubility and binding affinity to biological targets, making it valuable in creating potent drug candidates. Commonly employed in medicinal chemistry for constructing enzyme inhibitors and receptor ligands. Also utilized in the preparation of functionalized aromatic compounds for research in organic synthesis and drug discovery.

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...