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 1256834-36-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 4-bromo-5-chloropicolinate features a sterically accessible pyridine core bearing strategically positioned bromo and chloro substituents, enabling selective cross-coupling reactions. This bench-stable derivative integrates readily into synthetic sequences requiring halogen-directed functionalization, offering enhanced reactivity control in transition metal-catalyzed transformations.
Methyl 4-bromo-5-chloropicolinate serves as a versatile building block in synthetic organic chemistry, enabling regioselective cross-coupling reactions via its complementary halogenation pattern. The bromo group facilitates palladium-catalyzed coupling with boronic acids, while the chloro substituent offers orthogonal reactivity for subsequent functionalization. Its bench-stable methyl ester functionality simplifies purification and supports downstream transformations into bioactive heterocycles or pharmaceutical intermediates.
|
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: