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 443649-18-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(5-Aminopyridin-3-yl)methanol features a pyridine ring bearing both an amino group at the 5-position and a hydroxymethyl substituent at the 3-position, enabling dual functionalization. This scaffold integrates readily into bioconjugation workflows and serves as a key building block in medicinal chemistry due to its polar, hydrogen-bonding capabilities and compatibility with diverse reaction conditions.
(5-Aminopyridin-3-yl)methanol serves as a versatile building block for the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its pyridine core enables robust metal-catalyzed coupling reactions, while the pendant primary alcohol facilitates derivatization via esterification, etherification, or oxidation to aldehyde. The amine group exhibits strong nucleophilicity and moderate basicity, supporting efficient functionalization under mild conditions. Bench-stable and readily purified by recrystallization or chromatography, it functions effectively in multistep syntheses requiring orthogonal reactivity and compatibility with common protecting groups.
|
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: