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 114969-66-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromopyrimidine-4-carbonitrile features a bromine substituent at the 5-position and a nitrile group at the 4-position, enabling selective functionalization in heterocyclic synthesis. This electron-deficient pyrimidine scaffold integrates readily into pharmaceutical intermediates and materials precursors under standard conditions.
5-Bromopyrimidine-4-carbonitrile serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions and nucleophilic substitution at the bromine site. The nitrile group provides additional reactivity for functionalization, while the pyrimidine core offers structural rigidity and compatibility with medicinal chemistry applications. Its bench-stable nature and predictable reactivity make it ideal for modular synthesis workflows in API development and materials science.
|
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: