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 1245816-26-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(3-Methyl-1H-indazol-6-yl)boronic acid features a boronate moiety attached to a sterically accessible indazole scaffold, enabling efficient Suzuki-Miyaura coupling under mild conditions. This bench-stable reagent integrates readily into complex heterocyclic architectures, delivering high functional group tolerance and predictable reaction outcomes in medicinal chemistry applications.
(3-Methyl-1H-indazol-6-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds under mild conditions. Its stability, ease of handling, and compatibility with diverse functional groups make it ideal for medicinal chemistry applications and the synthesis of heterocyclic compounds. The boronic acid moiety facilitates reliable coupling with aryl halides and pseudohalides, supporting rapid library generation and scale-up.
|
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: