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 122234-46-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
tert-Butyl (2-iodoethyl)carbamate serves as a stable, bench-ready carbamate protecting group for primary amines. The iodoethyl moiety enables efficient copper-catalyzed coupling reactions, facilitating the introduction of diverse functional units. This reagent combines ease of handling with high reactivity in late-stage modifications.
tert-Butyl (2-iodoethyl)carbamate serves as a versatile building block in synthetic organic chemistry, enabling efficient introduction of both iodo and carbamate functionalities. Its stability under standard reaction conditions facilitates use in palladium-catalyzed cross-coupling reactions, while the tert-butyl carbamate group offers reliable protection for primary amines. The molecule functions effectively in C–N bond formation and heterocycle synthesis, with straightforward deprotection via acidolysis to yield the corresponding amine derivative.
|
GHS Pictogram :
|
GHS No : GHS05
|
|
Signal Word : Danger
|
UN#: 1759
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H302+H312+H332-H314
|
|
|
Precautionary Statements : P260-P264-P270-P271-P280-P301+P330+P331-P304+P340-P330-P362-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: