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 120747-85-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(2-Aminopyrimidin-5-yl)methanol features a pyrimidine core functionalized with an amino group at C2 and a hydroxymethyl substituent at C5, enabling integration into bioactive scaffolds. The pendant alcohol facilitates derivatization, while the electron-rich heterocycle supports metal coordination and hydrogen bonding in catalytic or medicinal applications. This bench-stable compound serves as a key intermediate for targeted molecular architectures.
(2-Aminopyrimidin-5-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds through straightforward functionalization. Its amine and alcohol functionalities offer orthogonal reactivity for coupling reactions, protecting group strategies, and heterocycle elaboration. The compound exhibits good bench stability and facilitates purification via standard chromatographic methods, supporting its utility in iterative synthesis workflows and API 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: