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 25177-85-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
A useful synthetic intermediate. 6-Bromonicotinaldehyde is used in wittig reaction. Hydrodehalogenation of 6-bromonicotinaldehyde to produce alcohol.
2,3-Dihydro-1H-indene-2-carboxylic acid serves as a versatile scaffold in medicinal chemistry and synthetic organic research. Its benzylic carboxylic acid functionality enables direct derivatization via amide coupling, esterification, or decarboxylation protocols. The rigid, partially saturated indene core provides structural constraint beneficial for target-specific ligand design, while the bench-stable, crystalline form facilitates handling and purification. Functions effectively in standard peptide coupling and heterocycle construction workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: