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 174072-89-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 2-amino-4-methyl-5-(4-nitrophenyl)thiophene-3-carboxylate features a fused thiophene core bearing a nitro-substituted aryl group and an aminoalkyl side chain, enabling direct incorporation into heterocyclic scaffolds. This electron-deficient, bench-stable building block facilitates transition-metal-catalyzed coupling reactions and serves as a key intermediate in the synthesis of bioactive thienyl compounds.
Ethyl 2-amino-4-methyl-5-(4-nitrophenyl)thiophene-3-carboxylate serves as a versatile building block in the synthesis of functionalized thiophene derivatives. The molecule combines a reactive amino group, a methyl substituent, and a nitroaryl moiety, enabling diverse transformations including Suzuki-Miyaura coupling, nucleophilic substitution, and reductive amination. Its bench-stable nature and compatibility with standard purification methods facilitate efficient incorporation into complex heterocyclic scaffolds relevant to medicinal chemistry and materials science.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: