CAS 126454-22-6

2,3'-Bipyridine, 1,2,3,6-tetrahydro-, (R)-

Description:

2,3'-Bipyridine, 1,2,3,6-tetrahydro-, (R)- is a chiral organic compound characterized by its bipyridine structure, which consists of two pyridine rings connected by a carbon bridge. This compound features a tetrahydro configuration, indicating that it has undergone partial hydrogenation, resulting in a saturated cyclic structure. The (R)- designation refers to its specific stereochemistry, which is important in determining its reactivity and interactions in various chemical environments. This substance is typically used in coordination chemistry and catalysis due to its ability to form complexes with metal ions. Its solubility properties can vary, but it is generally soluble in organic solvents. The presence of nitrogen atoms in the pyridine rings contributes to its basicity and potential as a ligand in various chemical reactions. As with many nitrogen-containing heterocycles, it may exhibit interesting biological activities, making it a subject of interest in medicinal chemistry. Safety data should be consulted for handling and storage, as with all chemical substances.

Formula: C₁₀H₁₂N₂

(R)-(+)-Anatabine

CAS: 126454-22-6

Formula: C₁₀H₁₂N₂

Color and Shape: Liquid

Molecular weight: 160.2157

Ref: IN-DA000ST8

(R)-(+)-Anatabine

CAS: 126454-22-6

(R)-(+)-Anatabine is an less active R-enantiomer of Anatabine. Anatabine is a potent agonist of α4β2 nAChR.

Formula: C₁₀H₁₂N₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 160.22

Ref: TM-T12636

(R)-(+)-Anatabine

Controlled Product

CAS: 126454-22-6

Applications The (R)-metabolite of Nicotine (N412420).
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Armstrong, D., et al.: Chirality, 11, 82 (1999), Carmella, S., et al.: Carcinogenesis, 21, 839 (2000),

Formula: C₁₀H₁₂N₂

Color and Shape: Neat

Molecular weight: 160.22

Ref: TR-A637490