CAS 5696-74-2

2-Naphthalenemethanol, a-(aminomethyl)-

Description:

2-Naphthalenemethanol, α-(aminomethyl)-, also known by its CAS number 5696-74-2, is an organic compound characterized by its naphthalene structure with a hydroxymethyl group and an amino group. This compound features a naphthalene ring system, which contributes to its aromatic properties, and the presence of both a hydroxyl (-OH) group and an amino (-NH2) group enhances its reactivity and solubility in polar solvents. The hydroxymethyl group can participate in hydrogen bonding, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and condensation reactions. Additionally, the amino group can act as a base, allowing for protonation under acidic conditions. This compound may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its structural characteristics suggest potential applications in the synthesis of more complex organic molecules, as well as in the study of structure-activity relationships in pharmacology. Overall, 2-Naphthalenemethanol, α-(aminomethyl)- is a versatile compound with significant implications in both synthetic and medicinal chemistry.

Formula: C₁₂H₁₃NO

2-amino-1-(naphthalen-2-yl)ethan-1-ol

CAS: 5696-74-2

Formula: C₁₂H₁₃NO

Color and Shape: Solid

Molecular weight: 187.2377

Ref: IN-DA00EN4U

2-(2-Amino-1-hydroxyethyl)naphthalene

CAS: 5696-74-2

2-(2-Amino-1-hydroxyethyl)naphthalene

Purity: 95%

Molecular weight: 187.24g/mol

Ref: 54-OR6056

2-Amino-1-(2-naphthyl)ethanol

CAS: 5696-74-2

Formula: C₁₂H₁₃NO

Purity: 97.0%

Color and Shape: Crystalline

Molecular weight: 187.242

Ref: 10-F067793

2-Amino-1-(2-naphthyl)-1-ethanol

CAS: 5696-74-2

2-Amino-1-(2-naphthyl)-1-ethanol (2NPE) is an atypical amino alcohol that is used as a pharmacological agent. It has been shown to have glucuronide and phenolic hydroxyl groups, which are reactive metabolites. 2NPE may be carcinogenic due to its ability to inhibit the activity of the enzyme glutathione reductase, which is involved in the detoxification of hydrogen peroxide and organic hydroperoxides. The metabolic pathways for 2NPE include sulfation by phenolic hydroxyl groups, which can lead to a residue of phenolic compounds in humans and animals. 2NPE has been found to have a thymic effect similar to natural n-substituted amino alcohols.

Formula: C₁₂H₁₃NO

Purity: Min. 95%

Molecular weight: 187.24 g/mol

Ref: 3D-FAA69674