CAS 870889-86-4

8-Azabicyclo[3.2.1]octane-8-carboxylic acid, 3-hydroxy-3-methyl-,1,1-dimethylethyl ester, (3-endo)-

Description:

8-Azabicyclo[3.2.1]octane-8-carboxylic acid, 3-hydroxy-3-methyl-, 1,1-dimethylethyl ester, (3-endo)-, is a bicyclic compound characterized by its unique azabicyclo structure, which incorporates a nitrogen atom into a bicyclic framework. This compound features a carboxylic acid moiety that is esterified with a tert-butyl group, contributing to its lipophilicity and potential biological activity. The presence of a hydroxyl group at the 3-position adds to its reactivity and solubility in polar solvents. The stereochemistry indicated by the (3-endo) designation suggests a specific spatial arrangement of the substituents, which can influence the compound's interaction with biological targets. This compound may exhibit pharmacological properties, making it of interest in medicinal chemistry and drug development. Its CAS number, 870889-86-4, allows for precise identification and retrieval of information regarding its synthesis, properties, and potential applications in various fields, including pharmaceuticals and organic synthesis.

Formula: C₁₃H₂₃NO₃

tert-butyl endo-3-hydroxy-3-methyl-8-azabicyclo[3.2.1]octane-8-carboxylate

CAS: 870889-86-4

Formula: C₁₃H₂₃NO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 241.3266

Ref: IN-DA01XA26

3-endo-Hydroxy-3-exo-methyl-8-azabicyclo[3.2.1]octane-8-carboxylic Acid t-Butyl Ester

Controlled Product

CAS: 870889-86-4

Applications 3-endo-Hydroxy-3-exo-methyl-8-azabicyclo[3.2.1]octane-8-carboxylic Acid t-Butyl Ester is an intermediate in the synthesis of ACP-105 (A115650). ACP-105 is a non-steroidal selective androgen receptor modulator used in the treatment of Alzheimer’s.
References George, S. et al.: ACS. Chem. Neurosci., 4, 1537 (2013)

Formula: C₁₃H₂₃NO₃

Color and Shape: Neat

Molecular weight: 241.327

Ref: TR-H998463