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 912761-33-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This imidazolylpiperidine methanol features a sterically accessible tertiary amine and a hydroxyl-bearing side chain, enabling efficient integration into bioactive scaffolds. The molecule combines moderate lipophilicity with hydrogen-bonding capacity, supporting solubility in common organic solvents and compatibility with diverse coupling reactions.
(1-Methyl-1H-imidazol-2-yl)(piperidin-4-yl)methanol serves as a versatile scaffold for medicinal chemistry campaigns, enabling efficient access to imidazole-piperidine hybrids. Its bench-stable nature and orthogonal functionality facilitate downstream derivatization, including amide coupling and alkylation reactions. The molecule functions as a key building block in the synthesis of bioactive heterocycles, particularly those targeting G-protein-coupled receptors and kinase modulators.
|
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: