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 125224-62-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This chiral diamine scaffold features a rigid bicyclic framework with defined stereochemistry at the 1S,4S positions, delivering high enantioselectivity in asymmetric catalysis. The dihydrobromide salt form enhances solubility and stability for use in synthetic transformations requiring precise stereocontrol.
(1S,4S)-2-Methyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide serves as a chiral, conformationally constrained diamine scaffold enabling efficient asymmetric synthesis. Its rigid bicyclic structure provides excellent stereocontrol in catalytic transformations, while the protonated amine centers offer strong basicity and improved solubility in polar media. The compound demonstrates high bench stability and facilitates straightforward purification, making it ideal for use in catalyst development, ligand design, and the construction of nitrogen-containing heterocycles relevant to medicinal chemistry.
|
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: