CAS 102547-84-2

9-METHYL-3,9-DIAZABICYCLO[4.2.1]NONANE

Description:

9-Methyl-3,9-diazabicyclo[4.2.1]nonane, with the CAS number 102547-84-2, is a bicyclic organic compound characterized by its unique structure, which includes a bicyclic framework and two nitrogen atoms incorporated into the ring system. This compound features a methyl group at the 9-position, contributing to its overall stability and reactivity. The presence of nitrogen atoms in the bicyclic structure imparts basic properties, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coordination with metal ions. Its bicyclic nature may also influence its conformational flexibility and steric interactions, which are important in determining its reactivity and potential applications in organic synthesis or medicinal chemistry. Additionally, the compound's solubility and stability in different solvents can vary, affecting its practical use in laboratory settings. Overall, 9-methyl-3,9-diazabicyclo[4.2.1]nonane is of interest for its structural features and potential applications in various chemical fields.

Formula: C₈H₁₆N₂

9-methyl-3,9-Diazabicyclo[4.2.1]nonane

CAS: 102547-84-2

Formula: C₈H₁₆N₂

Color and Shape: Liquid

Molecular weight: 140.2260

Ref: IN-DA0007P2

(1S,6R)-9-methyl-3,9-diazabicyclo[4.2.1]nonane dihydrochloride

CAS: 102547-84-2

Formula: C₈H₁₈Cl₂N₂

Purity: 95.0%

Molecular weight: 213.15

Ref: 10-F359988

9-Methyl-3,9-diazabicyclo[4.2.1]Nonane

CAS: 102547-84-2

Purity: 98%

Molecular weight: 140.2299957

Ref: 10-F765437

3,9-diazabicyclo[4.2.1]nonane, 9-methyl-

CAS: 102547-84-2

3,9-diazabicyclo[4.2.1]nonane, 9-methyl (DZB) is a spasmolytic drug that belongs to the group of aliphatic, aromatic acids, lactams and amides. It has been shown to have spasmolytic activity in animal experiments and has been used as an analgesic in humans. DZB is an analogue of 3,9-diazabicyclo[4.2.1]nonane (DZN) and is synthesized by reacting the corresponding sulfonyl chloride with a primary amine under acidic conditions followed by reduction with sodium borohydride or lithium aluminum hydride to yield the corresponding N-sulfonyl amide. This reaction can also be carried out using chlorosulfonic acid in place of sulfuric acid and an excess of primary amine over sulfonyl chloride.

Formula: C₈H₁₆N₂

Purity: Min. 95%

Molecular weight: 140.23 g/mol

Ref: 3D-CEA54784