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 1427158-38-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This bicyclic lactone features a rigid, strained framework with defined stereochemistry at the 1- and 5-positions. The carbonyl-bearing ring junction imparts high reactivity for selective transformations, while the oxygen bridge enhances solubility and modulates electronic properties. Ideal for asymmetric synthesis and molecular scaffold development.
(1S,5S)-3-Oxabicyclo[3.1.0]hexane-1-carboxylic acid serves as a rigid, bicyclic scaffold with defined stereochemistry, enabling precise spatial orientation in medicinal chemistry applications. The molecule features a carboxylic acid group that facilitates direct derivatization or conjugation, while the oxabicyclic core provides conformational stability and enhanced metabolic resistance. Its bench-stable nature and compatibility with standard coupling protocols make it a practical building block for targeted synthesis of bioactive molecules.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: