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 885167-81-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Bromo-5-methylnicotinaldehyde features a brominated pyridine ring fused with an aldehyde group, enabling direct functionalization in cross-coupling and cyclization reactions. The methyl substituent enhances electron density at the C5 position, while the bromo group provides a high-reactivity handle for palladium-catalyzed transformations. This bench-stable reagent integrates readily into complex heterocyclic architectures under standard conditions.
6-Bromo-5-methylnicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling direct incorporation of both halogen and aldehyde functionalities into heterocyclic scaffolds. Its bench-stable aldehyde group facilitates nucleophilic additions and condensation reactions, while the bromine atom supports palladium-catalyzed cross-coupling transformations. The methyl substituent enhances lipophilicity and provides a handle for further functionalization, making this compound well-suited for the synthesis of bioactive molecules and pharmaceutical intermediates.
|
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: