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 936-99-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-(tert-Butyl)cyclohexanone features a sterically hindered tert-butyl group attached to a cyclohexanone ring, enhancing its stability and influencing reactivity in synthetic transformations. This bulky substituent reduces undesired side reactions while maintaining solubility in common organic solvents. The ketone functionality enables direct use in nucleophilic additions, reductions, or as a building block for complex cyclic architectures. Its bench-stable nature supports reliable handling under standard conditions.
3-(tert-Butyl)cyclohexanone serves as a versatile scaffold in synthetic organic chemistry, enabling stereoselective functionalization at the C3 position due to the steric bias of the tert-butyl group. Its bench-stable ketone functionality facilitates nucleophilic additions, enolate formation, and reductive transformations, commonly employed in the synthesis of complex cyclic frameworks and bioactive molecules.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H227-H315-H319-H335
|
|
|
Precautionary Statements : P210-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P403-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: