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 142356-34-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
tert-Butyl (7-bromoheptyl)carbamate delivers a brominated alkyl chain with a stable carbamate protecting group, enabling selective functionalization in complex synthesis. The tert-butyl carbamate moiety ensures robust protection under standard conditions, while the terminal bromide facilitates palladium-catalyzed coupling reactions. This reagent integrates readily into multistep sequences requiring orthogonal handling and precise site-specific modification.
tert-Butyl (7-bromoheptyl)carbamate serves as a versatile protecting group for primary amines, enabling efficient introduction of bromoalkyl chains in synthetic sequences. The tert-butyl carbamate moiety provides excellent stability under basic conditions and facilitates mild deprotection via acidolysis. Its bromide functionality supports subsequent cross-coupling reactions, such as palladium-catalyzed Suzuki or Negishi transformations, making it a practical building block for functionalized alkylated scaffolds in medicinal chemistry and materials synthesis.
|
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 : P233-P260-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: