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 344331-90-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
N-Boc-2-Amino-6-bromopyridine features a bromine substituent at the pyridine ring's para position and a Boc-protected amine at the adjacent nitrogen, enabling seamless incorporation into diverse synthetic sequences. The electron-deficient pyridine core facilitates transition metal-catalyzed coupling reactions, while the bench-stable Boc group allows for straightforward deprotection under mild acidic conditions. This compound serves as a key intermediate in the synthesis of functionalized heterocycles and bioactive molecules.
N-Boc-2-Amino-6-bromopyridine serves as a versatile building block for the synthesis of brominated pyridine derivatives, enabling efficient late-stage functionalization in medicinal chemistry and agrochemical development. The Boc-protected amine exhibits excellent bench stability and compatibility with standard coupling reactions, while the ortho-bromo group facilitates palladium-catalyzed cross-coupling transformations. Its well-defined reactivity profile supports reliable access to complex heterocyclic scaffolds under routine laboratory conditions.
|
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: