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 41242-94-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Quinoxalin-2-ylmethanol features a rigid heteroaromatic core paired with a reactive benzylic alcohol group, enabling direct functionalization in synthetic sequences. This bench-stable scaffold integrates readily into bioactive molecule design, offering enhanced solubility and metabolic stability in medicinal chemistry applications.
Quinoxalin-2-ylmethanol serves as a versatile building block in medicinal chemistry, enabling efficient access to quinoxaline-based scaffolds prevalent in kinase inhibitors and bioactive heterocycles. Its primary alcohol functionality facilitates straightforward derivatization via etherification, esterification, or oxidation to the aldehyde, while maintaining compatibility with common protecting group strategies. The molecule exhibits excellent bench stability and ease of purification, making it well-suited for multi-step synthesis campaigns in API development and library generation.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H315-H319-H332-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: