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 136924-78-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
7-Bromonaphthalen-1-amine features a bromine substituent at the 7-position of the naphthalene core, enabling selective functionalization in cross-coupling reactions. The primary amine group provides a reactive handle for conjugation and derivatization. This bench-stable compound serves as a key intermediate in the synthesis of fluorescent dyes, pharmaceuticals, and advanced organic materials.
7-Bromonaphthalen-1-amine serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions and facilitating the construction of biaryl scaffolds. Its bromine and primary amine functionalities offer orthogonal reactivity for sequential functionalization. The compound exhibits good bench stability and is readily purified by recrystallization, making it well-suited for use in medicinal chemistry and process development workflows.
|
GHS Pictogram :
|
GHS No : GHS07,GHS08
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335-H341
|
|
|
Precautionary Statements : P201-P202-P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P308+P313-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: