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 1227599-26-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(3-Bromo-5-chloropyridin-2-yl)methanol features a pyridine core bearing bromo and chloro substituents at adjacent positions, enabling selective functionalization. The pendant hydroxymethyl group provides a handle for derivatization, facilitating incorporation into bioactive scaffolds. This bench-stable reagent combines high reactivity with predictable regiochemistry in cross-coupling and nucleophilic substitution processes.
(3-Bromo-5-chloropyridin-2-yl)methanol serves as a versatile building block for late-stage functionalization in medicinal chemistry and agrochemical synthesis. Its dual halogenation pattern enables selective cross-coupling reactions, while the benzylic alcohol functionality facilitates derivatization via oxidation, protection, or substitution. The compound exhibits excellent bench stability and compatibility with standard Pd-catalyzed transformations, making it ideal for constructing complex heterocyclic scaffolds under mild conditions.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: