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 53844-02-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Benzyl (2-bromoethyl)carbamate delivers a reactive bromoethyl handle for nucleophilic substitution, enabling efficient conjugation in peptide synthesis and bioconjugation workflows. The benzyl carbamate moiety provides stability under standard conditions while the β-bromide facilitates rapid functionalization. This reagent combines synthetic versatility with reliable handling in air and moisture-sensitive applications.
Benzyl (2-bromoethyl)carbamate serves as a versatile bifunctional building block in synthetic organic chemistry, enabling efficient introduction of both carbamate and bromoalkyl handles. It functions as a key intermediate in the synthesis of bioactive heterocycles and peptide mimetics, offering high stability under standard bench conditions. The bromoethyl moiety facilitates alkylation reactions with nucleophiles, while the benzyl carbamate group provides reliable protection for amines, supporting orthogonal functionalization strategies in complex molecule assembly.
|
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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: