CAS 3886-70-2

(+)-1-(1-Naphthyl)ethylamine

Description:

(+)-1-(1-Naphthyl)ethylamine, with the CAS number 3886-70-2, is an organic compound characterized by its amine functional group and a naphthyl substituent. This compound features a chiral center, which contributes to its optical activity, specifically in the (+) configuration. It is typically a colorless to pale yellow liquid or solid, depending on its form and purity. The presence of the naphthyl group imparts significant hydrophobic characteristics, influencing its solubility in organic solvents while making it less soluble in water. This compound is often utilized in organic synthesis and as a building block in the development of pharmaceuticals and agrochemicals. Its amine functionality allows for various chemical reactions, including alkylation and acylation, making it versatile in synthetic chemistry. Additionally, due to its structural features, it may exhibit biological activity, which can be of interest in medicinal chemistry. Proper handling and storage are essential, as with many amines, to ensure safety and stability.

Formula: C₁₂H₁₃N

InChI: InChI=1S/C12H13N/c1-9(13)11-8-4-6-10-5-2-3-7-12(10)11/h2-9H,13H2,1H3/t9-/m1/s1

InChI key: InChIKey=RTCUCQWIICFPOD-SECBINFHSA-N

SMILES: [C@H](C)(N)C=1C2=C(C=CC1)C=CC=C2

Synonyms:

• (+)-1-(1-Naphthyl)ethylamine
• (+)-1-(α-Naphthyl)ethylamine
• (+)-Naphthylethylamine
• (+)-[(R)-1-(Naphthalen-1-yl)ethyl]amine
• (+)-α-(1-Naphthyl)ethylamine
• (1R)-1-(1-Naphthyl)ethanamine
• (1R)-1-(naphthalen-1-yl)ethan-1-amine
• (1R)-1-Naphthalen-1-ylethanamine
• (1R)-1-naphthalen-1-ylethanaminium
• (R)-(+)-1-(α-Naphthyl)ethylamine
• (R)-(+)-α-(1-Naphthyl) ethylamine
• (R)-1-(1-Naphthalenyl)ethylamine
• (R)-1-(1-Naphthyl)ethanamine
• (R)-1-(Naphthalen-1-yl)ethan-1-amine
• (R)-1-(naphthalen-1-yl)ethanamine
• (R)-1-Naphthylethylamine
• (R)-α-Methyl-1-naphthalenemethanamine
• (αR)-α-Methyl-1-naphthalenemethanamine
• 1-(Naphthalen-1-Yl)Ethanamine
• 1-Naphthalenemethanamine, α-methyl-, (R)-
• 1-Naphthalenemethanamine, α-methyl-, (αR)-
• 1-Naphthalenemethylamine, α-methyl-, (R)-(+)-
• 2,2-Diphenylethanamine
• R-(+)-alpha-(1-Naphthyl)ethylamine
• d-1-(1-Naphthyl)ethylamine
• (R)-(+)-1-(1-Naphthyl) ethylamine
• (R)-(+)-1-(1-naphthyl) ethylamine

(R)-(+)-1-(1-Naphthyl)ethylamine

CAS: 3886-70-2

Formula: C₁₂H₁₃N

Purity: >99.0%(GC)

Color and Shape: Colorless to Yellow clear liquid

Molecular weight: 171.24

Ref: 3B-N0482

(R)-(+)-1-(1-Naphthyl)ethylamine, 99%

CAS: 3886-70-2

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₁₂H₁₄N

Purity: 99%

Color and Shape: Clear colorless to yellow, Liquid

Molecular weight: 172.25

Ref: 02-A16918

(R)-1-(Naphthalen-1-yl)ethanamine

CAS: 3886-70-2

Formula: C₁₂H₁₃N

Purity: 98%

Color and Shape: Liquid

Molecular weight: 171.2383

Ref: IN-DA003C49

(1R)-(+)-1-(Naphth-1-yl)ethylamine

CAS: 3886-70-2

(1R)-(+)-1-(Naphth-1-yl)ethylamine

Formula: C₁₂H₁₃N

Purity: 98%

Color and Shape: yellow liquid

Molecular weight: 171.24g/mol

Ref: 54-OR2650

Cinacalcet Impurity 33

CAS: 3886-70-2

Formula: C₁₂H₁₃N

Molecular weight: 171.24

Ref: 4Z-C-4097

(R)-(+)-1-(1-Naphthyl)ethylamine Cinacalcet Impurity A

CAS: 3886-70-2

Applications (R)-(+)-1-(1-Naphthyl)ethylamine is used in chiral synthesis in organic reactions including the synthesis of β-amino acids and the enantioselective of ketones to nitroolefins.
References Tsogoeva, S. et al.: Chem. Comm., 13, 1451 (2006); Lubell, W. et al.: Tetra. Asymm., 2, 543 (1991);

Formula: C₁₂H₁₃N

Color and Shape: Light Yellow Oily

Molecular weight: 171.24

Ref: TR-N378345

(R)-(+)-1-(1-Naphthyl)ethylamine

CAS: 3886-70-2

Formula: C₁₂H₁₃N

Purity: 96%

Color and Shape: Liquid, Clear

Molecular weight: 171.243

Ref: 10-F046443

(R)-(+)-1,1-Naphthyl ethylamine

CAS: 3886-70-2

(R)-(+)-1,1-Naphthyl ethylamine is a molecule that belongs to the class of chromatographic compounds. It has a carbonyl group, which is a substrate for amine modifiers and other chemical reactions. (R)-(+)-1,1-Naphthyl ethylamine can be used as a model system for epidermal growth factor (EGF) and chelate rings. The molecule has been shown to have growth factor activity, which may be due to its ability to bind to EGF receptors on cells.

Formula: C₁₂H₁₃N

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 171.24 g/mol

Ref: 3D-FN11785