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 317335-16-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 4-(bromomethyl)picolinate features a bromomethyl group at the pyridine ring's 4-position, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. This bench-stable reagent integrates readily into synthetic sequences requiring selective alkylation or chain extension, particularly in medicinal chemistry and heterocyclic synthesis.
Methyl 4-(bromomethyl)picolinate serves as a versatile building block for constructing bioactive heterocycles and pharmaceutical intermediates. The bromomethyl group enables efficient nucleophilic substitution, facilitating C–C and C–heteroatom bond formation under mild conditions. Its stability under standard bench handling and compatibility with diverse functional groups make it ideal for iterative synthesis workflows in medicinal chemistry and process development.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: