CAS 3082-62-0

(S)-(-)-A-(2-naphthyl)ethylamine

Description:

(S)-(-)-A-(2-naphthyl)ethylamine, with the CAS number 3082-62-0, is an organic compound characterized by its chiral structure, which includes a naphthyl group attached to an ethylamine backbone. This compound is typically a colorless to pale yellow liquid or solid, depending on its form and purity. It exhibits basic properties due to the presence of the amine functional group, allowing it to participate in various chemical reactions, including alkylation and acylation. The naphthyl moiety contributes to its hydrophobic characteristics, influencing its solubility in organic solvents while being less soluble in water. This compound is of interest in medicinal chemistry and drug development, particularly for its potential biological activity, including interactions with neurotransmitter systems. Additionally, its chirality may impart specific pharmacological properties, making it relevant in the study of enantiomeric effects in biological systems. Proper handling and storage are essential due to its potential reactivity and the need for safety precautions when working with amines.

Formula: C₁₂H₁₃N

InChI: InChI=1S/C12H13N/c1-9(13)11-7-6-10-4-2-3-5-12(10)8-11/h2-9H,13H2,1H3/t9-/m0/s1

InChI key: InChIKey=KHSYYLCXQKCYQX-VIFPVBQESA-N

SMILES: [C@@H](C)(N)C1=CC2=C(C=C1)C=CC=C2

Synonyms:

• (-)-1-(2-Naphthyl)ethylamine
• (-)-α-2-Naphthylethylamine
• (1S)-1-(2-Naphthyl)ethanamine
• (1S)-1-(2-Naphthyl)ethylamine
• (1S)-1-(Naphthalen-2-yl)ethan-1-amine
• (1S)-1-(naphthalen-2-yl)ethanamine
• (1S)-1-Naphthalen-2-ylethanamine
• (S)-(-)-1-(2-Naphthyl)ethylamine
• (S)-(-)-1-(Naphthalen-2-yl)ethylamine
• (S)-1-(Naphthalen-2-yl)ethanamine
• (S)-1-(β-Naphthyl)ethylamine
• (S)-α-Methyl-2-naphthalenemethanamine
• (αS)-α-Methyl-2-naphthalenemethanamine
• 2-Naphthalenemethanamine α-methyl-, (αS)-
• 2-Naphthalenemethanamine, α-methyl-, (S)-
• 2-Naphthalenemethylamine, α-methyl-, (S)-(-)-

(S)-(-)-1-(2-Naphthyl)ethylamine, ChiPros 99+%, ee 99+%

CAS: 3082-62-0

(S)-(-)-1-(2-Naphthyl)ethylamine is used in asymmetric synthesis. It is also used in the preparation of thiourea compounds using chiral amine, which is used as a bifunctional catalyst for the Strecker and nitro-Michael reactions. Further, it acts as a chiral building block and chiral resolution reag

Formula: C₁₂H₁₃N

Purity: 99+%

Color and Shape: White to pale yellow, Crystals or powder or crystalline powder or fused/lumpy solid

Molecular weight: 171.24

Ref: 02-L17024

(S)-1-(Naphthalen-2-yl)ethanamine

CAS: 3082-62-0

Formula: C₁₂H₁₃N

Purity: 97%

Color and Shape: Solid

Molecular weight: 171.2383

Ref: IN-DA003CCZ

(S)-(-)-1-(2-Naphthyl)ethylamine

CAS: 3082-62-0

(S)-(-)-1-(2-Naphthyl)ethylamine

Purity: 98%

Molecular weight: 171.24g/mol

Ref: 54-OR936986

(S)-1-(2-Naphthyl)ethylamine

CAS: 3082-62-0

Formula: C₁₂H₁₃N

Purity: >98.0%(GC)(T)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 171.24

Ref: 3B-N0726

Evocalcet Impurity 59

CAS: 3082-62-0

Formula: C₁₂H₁₃N

Molecular weight: 171.24

Ref: 4Z-E-204062

(S)-1-(Naphthalen-2-yl)ethanamine

CAS: 3082-62-0

Formula: C₁₂H₁₃N

Purity: 95%

Color and Shape: Solid, Solidified mass or fragments

Molecular weight: 171.243

Ref: 10-F222927

(S)-1-(2-Naphthyl)ethylamine

CAS: 3082-62-0

(S)-1-(2-Naphthyl)ethylamine is a selective allosteric modulator of the prostacyclin receptor. It binds to the active site of the receptor and activates it, leading to increased production of prostacyclin. This activation leads to vasodilation and inhibition of platelet aggregation. (S)-1-(2-Naphthyl)ethylamine has been shown to be effective in suppressing vascular hypertrophy in cho-k1 cells. The drug inhibits the production of TNF-α and IL-6 by these cells, which may be due to its ability to induce apoptosis or suppress protein synthesis through inhibition of mRNA translation.

Formula: C₁₂H₁₃N

Purity: Min. 95%

Molecular weight: 171.24 g/mol

Ref: 3D-FN60265