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 73013-69-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Methylquinoline-6-carbonitrile features a sterically hindered quinoline core with a nitrile group at the 6-position, enabling robust coupling reactions. The methyl substituent enhances electron density at the C2 position, facilitating selective functionalization in transition-metal-catalyzed transformations. This bench-stable heterocycle serves as a key scaffold in medicinal chemistry and materials science.
2-Methylquinoline-6-carbonitrile serves as a versatile building block in medicinal chemistry and catalytic synthesis, offering a rigid heteroaromatic scaffold with orthogonal functional handles. The nitrile group enables subsequent transformations such as amidation, hydrolysis, or nucleophilic addition, while the methyl substituent provides steric definition and potential for further functionalization. Its stability under standard reaction conditions and compatibility with common coupling protocols facilitate integration into complex molecular architectures.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: