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 3438-52-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromo-4-hydroxy-6-methylpyrimidine features a strategically positioned bromo group and hydroxyl moiety on a pyrimidine scaffold, enabling direct functionalization in cross-coupling and derivatization workflows. The methyl substituent enhances solubility and stability under standard conditions. This heterocycle serves as a key intermediate for bioactive molecule synthesis.
5-Bromo-4-hydroxy-6-methylpyrimidine serves as a versatile building block in heterocyclic synthesis, enabling direct functionalization at the C4 hydroxyl and C5 bromine positions. Its stability under standard reaction conditions facilitates efficient coupling reactions and nucleophilic substitutions. The methyl group enhances solubility and provides a handle for further derivatization. This compound functions reliably in the construction of pyrimidine-based scaffolds relevant to medicinal chemistry and agrochemical 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: