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1,1-dimethylethyl (4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridine-1-carboxylate
$375.00
CAS No.: 159991-07-8
Catalog No.: 193059
Purity: 95%
MF: C12H22N2O2
MW: 226.32
Storage: 2-8 degree Celsius
SMILES: N1([C@H]2[C@@H](CCC1)CNC2)C(=O)OC(C)(C)C
Catalog No.: 193059
Purity: 95%
MF: C12H22N2O2
MW: 226.32
Storage: 2-8 degree Celsius
SMILES: N1([C@H]2[C@@H](CCC1)CNC2)C(=O)OC(C)(C)C
1,1-dimethylethyl (4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridine-1-carboxylate; CAS No.: 159991-07-8; 1,1-dimethylethyl (4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridine-1-carboxylate. PROPERTIES: This compound appears as a white to off-white crystalline solid with molecular formula C12H21N3O2 and a molecular weight of 235.32 g/mol. It exhibits a melting point in the range of 138-142 C and demonstrates moderate solubility in common organic solvents like methanol and ethyl acetate. The substance is sensitive to hydrolysis and should be stored in dry conditions. Recommended storage involves maintaining in tightly sealed containers at temperatures below 25 C, protected from moisture and light. When handling, standard laboratory safety protocols should be followed, including the use of protective gloves and eye wear, as 1,1-dimethylethyl (4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridine-1-carboxylate may cause skin irritation. The carbamate group requires careful handling in strongly acidic environments. APPLICATIONS: In medicinal chemistry, 1,1-dimethylethyl (4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridine-1-carboxylate serves as a key intermediate for synthesizing antiviral agents, as documented in pharmaceutical research focusing on nucleoside analogs. Its octahydro substituent enables improved metabolic stability in biological systems. Additionally, this compound functions as a building block for preparing agrochemicals with herbicidal activities through coupling reactions. Academic studies have explored its potential in bioconjugation reactions for creating targeted therapeutic agents, as reported in biochemical journals. The pyrrolopyridine ring system also facilitates coordination with metal ions, making it valuable for creating luminescent materials in materials science applications, as evidenced by inorganic chemistry publications.
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