4-Nitrobenzaldehyde semicarbazone is an organic compound derived from the reaction of 4-nitrobenzaldehyde and semicarbazide. It is characterized by the presence of a semicarbazone functional group, which is formed through the condensation of a carbonyl compound with a semicarbazide. This compound typically appears as a crystalline solid and is known for its yellow to orange coloration. It is soluble in organic solvents such as ethanol and methanol but has limited solubility in water. The presence of the nitro group on the benzaldehyde ring contributes to its reactivity and can influence its chemical properties, including its ability to participate in various chemical reactions, such as nucleophilic substitutions and reductions. 4-Nitrobenzaldehyde semicarbazone is often utilized in organic synthesis and as an intermediate in the preparation of other chemical compounds. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry and pharmacological studies. Proper handling and storage are essential due to its potential toxicity and reactivity.

4-nitrobenzaldehyde semicarbazone

5315-87-7: 4-Nitrobenzaldehyde semicarbazone is an organic compound derived from the reaction of 4-nitrobenzaldehyde and semicarbazide. It is characterized by the presence of a semicarbazone functional group, which is formed through the condensation of a carbonyl compound with a semicarbazide. This compound typically appears as a crystalline solid and is known for its yellow to orange coloration. It is soluble in organic solvents such as ethanol and methanol but has limited solubility in water. The presence of the nitro group on the benzaldehyde ring contributes to its reactivity and can influence its chemical properties, including its ability to participate in various chemical reactions, such as nucleophilic substitutions and reductions. 4-Nitrobenzaldehyde semicarbazone is often utilized in organic synthesis and as an intermediate in the preparation of other chemical compounds. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry and pharmacological studies. Proper handling and storage are essential due to its potential toxicity and reactivity.

CAS 5315-87-7

4-nitrobenzaldehyde semicarbazone

(E)-2-(4-Nitrobenzylidene)hydrazinecarboxamide

Ref: 54-OR310620

2-(4-NITROBENZYLIDENE)HYDRAZINECARBOXAMIDE

Ref: 10-F475612