CAS 82409-04-9

1,1-Dimethylethyl N-[3-[(3-aminopropyl)amino]propyl]carbamate

Description:

1,1-Dimethylethyl N-[3-[(3-aminopropyl)amino]propyl]carbamate, also known by its CAS number 82409-04-9, is a chemical compound characterized by its complex structure that includes a carbamate functional group. This compound features a tert-butyl group, which contributes to its steric hindrance, and an amino group that enhances its potential for biological activity. The presence of multiple amine functionalities suggests that it may engage in hydrogen bonding, influencing its solubility and reactivity. Typically, compounds like this can exhibit properties such as moderate to high polarity, which may affect their interaction with biological systems. Additionally, the presence of amino groups often indicates potential applications in pharmaceuticals or as intermediates in organic synthesis. The stability of the carbamate linkage can also play a crucial role in its reactivity and degradation pathways. Overall, the characteristics of this compound suggest it may have significant utility in various chemical and biological applications, although specific behavior would depend on environmental conditions and the presence of other reactants.

Formula: C₁₁H₂₅N₃O₂

InChI: InChI=1S/C11H25N3O2/c1-11(2,3)16-10(15)14-9-5-8-13-7-4-6-12/h13H,4-9,12H2,1-3H3,(H,14,15)

InChI key: InChIKey=DZFPOUXCPWBUDA-UHFFFAOYSA-N

SMILES: N(C(OC(C)(C)C)=O)CCCNCCCN

Synonyms:

• tert-Butyl [3-[(3-aminopropyl)amino]propyl]carbamate
• Carbamic acid, N-[3-[(3-aminopropyl)amino]propyl]-, 1,1-dimethylethyl ester
• Carbamic acid, [3-[(3-aminopropyl)amino]propyl]-, 1,1-dimethylethyl ester
• 1,1-Dimethylethyl N-[3-[(3-aminopropyl)amino]propyl]carbamate