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 72996-65-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-(2-Bromoethyl)pyridine hydrobromide delivers a reactive bromoalkyl handle adjacent to a pyridine nitrogen, enabling efficient coupling in nucleophilic substitution reactions. The hydrobromide salt enhances solubility and stability in polar solvents, facilitating straightforward incorporation into functionalized polymers, bioconjugates, and heterocyclic architectures under mild conditions.
2-(2-Bromoethyl)pyridine hydrobromide serves as a versatile bifunctional building block for heterocyclic synthesis, enabling efficient alkylation and coupling reactions. The bromoethyl side chain facilitates nucleophilic substitution with amines, thiols, and other soft nucleophiles, while the pyridinium moiety enhances solubility and reactivity in polar media. This stable, bench-ready reagent simplifies purification and is well-suited for constructing pharmaceutically relevant scaffolds via straightforward functional group interconversions.
|
GHS Pictogram :
|
GHS No : GHS05,GHS07
|
|
Signal Word : Danger
|
UN#: 1759
|
|
Class : 8
|
Packing Group : Ⅱ
|
|
Hazard Statements : H302-H314
|
|
|
Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P363-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: