Tert-butyl 4-(3-nitropyridin-4-yl)piperazine-1-carboxylate, with the CAS number 608142-93-4, is a chemical compound characterized by its complex structure, which includes a piperazine ring, a tert-butyl group, and a nitropyridine moiety. This compound is typically a solid at room temperature and is soluble in organic solvents, reflecting its moderate polarity due to the presence of both hydrophobic and hydrophilic groups. The nitro group on the pyridine ring contributes to its electronic properties, potentially influencing its reactivity and interactions in biological systems. The tert-butyl ester group enhances its lipophilicity, which may affect its pharmacokinetic properties if used in medicinal chemistry. Additionally, the compound may exhibit biological activity, making it of interest in drug discovery and development. Its synthesis involves standard organic reactions, including esterification and substitution reactions, which are common in the preparation of complex organic molecules. Proper handling and storage are essential due to the potential hazards associated with the nitro group.

tert-butyl 4-(3-nitropyridin-4-yl)piperazine-1-carboxylate

608142-93-4: Tert-butyl 4-(3-nitropyridin-4-yl)piperazine-1-carboxylate, with the CAS number 608142-93-4, is a chemical compound characterized by its complex structure, which includes a piperazine ring, a tert-butyl group, and a nitropyridine moiety. This compound is typically a solid at room temperature and is soluble in organic solvents, reflecting its moderate polarity due to the presence of both hydrophobic and hydrophilic groups. The nitro group on the pyridine ring contributes to its electronic properties, potentially influencing its reactivity and interactions in biological systems. The tert-butyl ester group enhances its lipophilicity, which may affect its pharmacokinetic properties if used in medicinal chemistry. Additionally, the compound may exhibit biological activity, making it of interest in drug discovery and development. Its synthesis involves standard organic reactions, including esterification and substitution reactions, which are common in the preparation of complex organic molecules. Proper handling and storage are essential due to the potential hazards associated with the nitro group.

CAS 608142-93-4

tert-butyl 4-(3-nitropyridin-4-yl)piperazine-1-carboxylate

1-Piperazinecarboxylic acid, 4-(3-nitro-4-pyridinyl)-, 1,1-dimethylethylester

Ref: IN-DA01DTMG

tert-Butyl 4-(3-nitropyridin-4-yl)piperazine-1-carboxylate

Ref: 10-F614445