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 52651-16-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Bromo-2,3-dihydro-1H-indene-1-carboxylic acid features a brominated indene core with a carboxylic acid handle, enabling direct functionalization in synthetic routes. The electron-deficient aryl bromide facilitates cross-coupling reactions, while the saturated indene ring offers enhanced stability and solubility under standard conditions. This compound serves as a versatile intermediate for medicinal chemistry and materials synthesis.
6-Bromo-2,3-dihydro-1H-indene-1-carboxylic acid serves as a versatile building block in medicinal chemistry and synthetic organic chemistry. Its structure combines a brominated aromatic ring with a carboxylic acid functional group, enabling facile Suzuki-Miyaura coupling and derivatization via esterification or amide formation. The molecule exhibits good bench stability and facilitates access to substituted indene scaffolds commonly found in bioactive molecules.
|
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: