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 1932616-77-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This chiral pyrrolidinol derivative features a fluorinated, methyl-substituted ring system that enhances metabolic stability and membrane permeability. The pendant hydroxymethyl group enables direct functionalization or conjugation in synthetic routes. This scaffold integrates readily into bioactive molecules, particularly in CNS-targeted pharmaceutical development, where its steric profile and polarity support target engagement.
((2S,4S)-4-Fluoro-1-methylpyrrolidin-2-yl)methanol serves as a versatile chiral building block in medicinal chemistry, enabling the construction of fluorinated pyrrolidine scaffolds found in bioactive molecules. Its bench-stable nature and compatibility with standard coupling and functionalization protocols facilitate efficient synthesis of targeted analogs. The presence of both hydroxyl and methyl groups provides orthogonal handles for derivatization, while the stereochemistry ensures predictable stereochemical outcomes in downstream transformations.
|
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: