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 161833-42-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 3-amino-4-bromothiophene-2-carboxylate features a brominated thiophene core with complementary amino and ester functionalities, enabling direct integration into cross-coupling and heterocyclic synthesis. The electron-rich amine group facilitates nucleophilic transformations, while the bromine serves as a reliable coupling handle under palladium catalysis. This bench-stable scaffold supports rapid diversification in medicinal chemistry and materials development.
Methyl 3-amino-4-bromothiophene-2-carboxylate serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its bromine handle. The amino and ester functionalities provide orthogonal reactivity, facilitating sequential transformations in medicinal chemistry and materials science. Bench-stable and readily purified by column chromatography, it supports efficient access to substituted thiophene scaffolds relevant to API development.
|
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: