(2,6-Dibromophenyl)methanesulfonyl chloride

95%

Reagent Code: #180345
fingerprint
CAS Number 256651-55-5

science Other reagents with same CAS 256651-55-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 348.43 g/mol
Formula C₇H₅Br₂ClO₂S
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a sulfonylating agent in organic reactions. It enables the introduction of sulfonyl groups into heterocyclic or aromatic systems, enhancing molecular stability and reactivity in drug design. Its bromine substituents allow for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in building complex molecules. It is also employed in the development of bioactive compounds, including kinase inhibitors and antimicrobial agents, due to its ability to modulate electronic and steric properties in target molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿24,610.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(2,6-Dibromophenyl)methanesulfonyl chloride
No image available

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a sulfonylating agent in organic reactions. It enables the introduction of sulfonyl groups into heterocyclic or aromatic systems, enhancing molecular stability and reactivity in drug design. Its bromine substituents allow for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in building complex molecules. It is also employed in the d

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a sulfonylating agent in organic reactions. It enables the introduction of sulfonyl groups into heterocyclic or aromatic systems, enhancing molecular stability and reactivity in drug design. Its bromine substituents allow for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in building complex molecules. It is also employed in the development of bioactive compounds, including kinase inhibitors and antimicrobial agents, due to its ability to modulate electronic and steric properties in target molecules.

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...