Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 1058741-91-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,6-Dichloropyridine-4-sulfonyl chloride features a reactive sulfonyl chloride group flanked by two chlorine atoms at the 2 and 6 positions of the pyridine ring. This electron-deficient scaffold enables selective acylation of nucleophiles in synthetic transformations. The molecule exhibits enhanced stability under standard conditions while maintaining high reactivity toward amines and alcohols, facilitating efficient incorporation into functionalized heterocycles and bioactive intermediates.
2,6-Dichloropyridine-4-sulfonyl chloride serves as a versatile building block for sulfonamide synthesis, enabling efficient introduction of the pyridine-4-sulfonyl motif into pharmaceutical and agrochemical scaffolds. Its reactivity is well-documented in standard coupling protocols, with the sulfonyl chloride group readily reacting with amines under mild conditions to form stable sulfonamide linkages. The dichloro substitution pattern enhances electrophilicity at the sulfonyl center while maintaining bench stability and ease of purification, making it suitable for scalable, high-yield transformations in medicinal chemistry workflows.
|
GHS Pictogram :
|
GHS No : GHS05,GHS07
|
|
Signal Word : Danger
|
UN#: 3261
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H302-H314-H335
|
|
|
Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P312-P330-P363-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: