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 7467-35-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This bench-stable benzimidazole derivative features a methyl-substituted heterocyclic core paired with a reactive hydroxymethyl group. The functionalized side chain enables direct incorporation into bioconjugation workflows and modular synthesis of pharmaceutical intermediates, offering enhanced solubility in polar solvents and compatibility with standard coupling conditions.
(1-Methyl-1H-benzoimidazol-2-yl)-methanol serves as a versatile building block for heterocyclic synthesis, enabling efficient access to bioactive scaffolds. Its benzimidazole core provides enhanced metabolic stability and favorable pharmacophore properties, while the pendant alcohol functions as a handle for derivatization via esterification, ether formation, or oxidation. The compound exhibits good bench stability and is compatible with standard purification methods, facilitating integration into medicinal chemistry and process development workflows.
|
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-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: