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 186663-83-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This fluorenylmethyl carbamate derivative features a reactive bromopropyl handle for facile conjugation. The 9-fluorenylmethyl group provides excellent solubility and stability during solid-phase synthesis, while the pendant bromide enables efficient coupling reactions in peptide and oligonucleotide chemistry workflows.
(9H-Fluoren-9-yl)methyl (3-bromopropyl)carbamate serves as a versatile bifunctional building block in peptide and oligonucleotide synthesis, enabling efficient conjugation via its bromoalkyl handle. The fluorenylmethoxycarbonyl (Fmoc) group provides orthogonal protection for amines, while the pendant 3-bromopropyl moiety facilitates nucleophilic substitution with thiols, amines, or azide derivatives. Its bench-stable nature and compatibility with standard purification methods make it ideal for modular assembly of bioconjugates and functionalized scaffolds.
|
GHS Pictogram :
N/A
|
GHS No : N/A
|
|
Signal Word : N/A
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : N/A
|
|
|
Precautionary Statements : N/A
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: