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 1975-51-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Methyl-4-nitrobenzoic acid features a nitro group at the para position relative to the carboxylic acid, enhancing electrophilicity for downstream functionalization. The methyl substituent introduces steric and electronic modulation, improving solubility in organic solvents while maintaining stability under standard bench conditions. This structure facilitates direct incorporation into pharmaceutical intermediates and fine chemical syntheses.
2-Methyl-4-nitrobenzoic acid serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted benzoic acid derivatives. Its ortho-methyl and para-nitro substituents provide complementary reactivity for selective functionalization, while the carboxylic acid group facilitates direct coupling reactions or derivatization. The compound exhibits good bench stability and is readily purified by recrystallization, supporting reliable use in multi-step syntheses.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H317
|
|
|
Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: