tert-butyl (4R)-4-aminoazepane-1-carboxylate

tert-butyl (4R)-4-aminoazepane-1-carboxylate

1-benzyl-5-bromoazepan-4-one hydrochloride

1-benzyl-5-bromoazepan-4-one hydrochloride

tert-butyl 1,4-diazepane-1-carboxylate

$300.00
CAS No.: 112275-50-0
Catalog No.: 196106
Purity: 95%
MF: C10H20N2O2
MW: 200.282
Storage: 2-8 degree Celsius
SMILES: N1(CCNCCC1)C(=O)OC(C)(C)C
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196106
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tert-butyl 1,4-diazepane-1-carboxylate; CAS No.: 112275-50-0; tert-butyl 1,4-diazepane-1-carboxylate. PROPERTIES: tert-butyl 1,4-diazepane-1-carboxylate is a viscous liquid with a molecular weight of approximately 198.2 g/mol. It has a boiling point around 140-150 C at reduced pressure and a density of approximately 1.05 g/cm?. The compound is moderately soluble in common organic solvents like ethyl acetate and methanol but is practically insoluble in water. The tert-butyl group provides steric protection to the carbamate linkage. For proper storage, keep in a tightly sealed container at room temperature away from heat and moisture. Safety: This compound may cause serious eye irritation. In case of contact with eyes, rinse cautiously with water for several minutes and remove contact lenses if present. Use explosion-proof ventilation and lighting if handling large quantities. APPLICATIONS: In pharmaceutical research, tert-butyl 1,4-diazepane-1-carboxylate serves as a protected amino acid derivative. The Boc group protects the amine during synthetic manipulations. In organic synthesis, it is used as a building block for creating bioactive molecules. The diazepane ring provides structural features that enhance binding to biological targets. In materials science, derivatives of this compound are explored for creating molecular machines. The combination of the diazepane ring and the carbamate group creates a scaffold that can undergo conformational changes. These applications are supported by research in medicinal chemistry journals and materials science publications.

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