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 194491-44-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate moiety integrates a 5-(2-thienyl)-3-isoxazolyl group with a terminal alcohol, enabling efficient coupling in cross-coupling reactions. The thiophene isolevelling electron density enhances reactivity, while the isoxazole ring provides stability under standard conditions.
[5-(2-Thienyl)-3-isoxazolyl]methanol serves as a versatile building block for heterocyclic synthesis, enabling efficient access to biologically relevant scaffolds. Its isoxazole ring fused with a thienyl moiety provides enhanced electronic delocalization and metabolic stability. The pendant primary alcohol facilitates straightforward derivatization—via oxidation, protection, or coupling reactions—while maintaining excellent bench stability and compatibility with standard synthetic protocols.
|
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: