4-cyano-3-methylbenzaldehyde
$200.00
CAS No.: 27613-35-0
Catalog No.: 194060
Purity: 95%
MF: C9H7NO
MW: 145.161
Storage: 2-8 degree Celsius
SMILES: C(#N)C1=C(C=C(C=O)C=C1)C
Catalog No.: 194060
Purity: 95%
MF: C9H7NO
MW: 145.161
Storage: 2-8 degree Celsius
SMILES: C(#N)C1=C(C=C(C=O)C=C1)C
4-cyano-3-methylbenzaldehyde; CAS No.: 27613-35-0; 4-cyano-3-methylbenzaldehyde. PROPERTIES: 4-cyano-3-methylbenzaldehyde is a crystalline solid with a molecular weight of 165.18 g/mol. It typically exhibits a melting point in the range of 68-71 C and limited water solubility, though it dissolves readily in organic solvents such as methanol, ethanol, and dichloromethane. The compound contains reactive functional groups including an aldehyde group, cyano group, and methyl group, which contribute to its chemical versatility. For optimal storage, it should be kept in a tightly sealed container at temperatures below 20 C, preferably under inert atmosphere to prevent potential oxidation of the aldehyde group. Safety considerations include wearing appropriate protective clothing, gloves, and eye/face protection to minimize exposure risk. The compound may cause eye irritation and skin irritation, and in case of accidental ingestion, immediate medical attention is advised. The aldehyde group is highly reactive and may form irreversible conjugates with biomolecules, so appropriate precautions should be taken. APPLICATIONS: 4-cyano-3-methylbenzaldehyde serves as a valuable intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its unique substitution pattern allows for selective derivatization, making it suitable for constructing bioactive scaffolds, as reported in medicinal chemistry literature. In materials science, the compound functions as a building block for certain types of liquid crystalline materials and conductive polymers. The presence of the aldehyde group provides a convenient handle for further functionalization, enabling the formation of various derivatives such as imines and hemiacetals. Additionally, it is utilized in the preparation of specialty dyes and pigments, where its structure contributes to desired solubility and stability characteristics. Through chemical modification of the aldehyde group, it can be converted into various functionalized derivatives, expanding its application scope in organic synthesis. The cyano group can be reduced to a methyl group or hydrolyzed to a carboxylic acid, providing additional synthetic utility.
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