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 1443983-86-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This fluoromethyl-substituted azetidine derivative features a labile hydroxyl group and a strained four-membered ring, enabling selective bioorthogonal reactivity. The fluoromethyl moiety enhances metabolic stability while maintaining favorable solubility, making it ideal for probing dynamic biological systems under physiological conditions.
2-[3-(Fluoromethyl)azetidin-1-yl]ethan-1-ol serves as a versatile building block in medicinal chemistry, enabling the introduction of a fluoromethyl-substituted azetidine motif with enhanced metabolic stability. The molecule combines a polar hydroxyl group with a strained azetidine ring and a reactive fluoromethyl handle, facilitating downstream functionalization via nucleophilic substitution or coupling reactions. Its bench-stable nature and compatibility with standard purification methods support efficient integration into complex synthetic sequences for API development.
|
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: