tert-butyl trans-3,4-diaminopyrrolidine-1-carboxylate
$300.00
CAS No.: 2173182-42-6
Catalog No.: 193011
Purity: 95%
MF: C9H19N3O2
MW: 201.27
Storage: 2-8 degree Celsius
SMILES: N[C@@H]1CN(C[C@H]1N)C(=O)OC(C)(C)C
Catalog No.: 193011
Purity: 95%
MF: C9H19N3O2
MW: 201.27
Storage: 2-8 degree Celsius
SMILES: N[C@@H]1CN(C[C@H]1N)C(=O)OC(C)(C)C
tert-butyl trans-3,4-diaminopyrrolidine-1-carboxylate; CAS No.: 2173182-42-6; tert-butyl trans-3,4-diaminopyrrolidine-1-carboxylate. PROPERTIES: This compound appears as a white crystalline powder with molecular formula C11H21N3O2 and a molecular weight of 227.31 g/mol. It demonstrates a melting point in the range of 138-142 C and shows moderate solubility in common organic solvents like methanol and ethyl acetate. The substance is sensitive to acidic hydrolysis and should be stored in neutral conditions. Recommended storage involves maintaining in tightly sealed containers at temperatures below 20 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 tert-butyl trans-3,4-diaminopyrrolidine-1-carboxylate may release irritating vapors upon heating. The amino groups require careful handling in strongly acidic environments. APPLICATIONS: In medicinal chemistry, tert-butyl trans-3,4-diaminopyrrolidine-1-carboxylate serves as a key intermediate for synthesizing antiviral agents, as documented in pharmaceutical research focusing on nucleoside analogs. Its amino substituents enable formation of bioactive amides through amidation reactions. 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 pyrrolidine ring system also facilitates coordination with metal ions, making it valuable for creating coordination polymers in materials science applications, as evidenced by structural chemistry publications.
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