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 21651-84-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This chiral cyclohexanol derivative features a methylamino group at the 2-position and a hydroxyl moiety at the 1-position, enabling precise stereochemical control in asymmetric synthesis. The (1S,2S) configuration imparts distinct conformational rigidity and directional polarity, facilitating its use as a scaffold in medicinal chemistry and catalyst design.
(1S,2S)-2-(methylamino)cyclohexan-1-ol serves as a chiral building block for the synthesis of bioactive molecules, leveraging its rigid cyclohexane scaffold and stereodefined amino-alcohol functionality. The molecule exhibits bench stability, facilitates efficient derivatization via amine and hydroxyl groups, and functions effectively in asymmetric synthesis, particularly in the construction of nitrogen-containing heterocycles and pharmaceutical intermediates requiring defined stereochemistry.
|
GHS Pictogram :
N/A
|
GHS No : N/A
|
|
Signal Word : N/A
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : N/A
|
|
|
Precautionary Statements : N/A
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: