CAS 3082-62-0
:(S)-(-)-A-(2-naftil)etilamina
Fórmula: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
Clave InChI:InChIKey=KHSYYLCXQKCYQX-VIFPVBQESA-N
SMILES:[C@@H](C)(N)C1=CC2=C(C=C1)C=CC=C2
Sinónimos:- (-)-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)-(-)-
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(S)-1-(2-Naphthyl)ethylamine
CAS:Fórmula:C12H13NPureza:>98.0%(GC)(T)Forma y color:White to Light yellow powder to crystalPeso molecular:171.24(S)-(-)-1-(2-Naphthyl)ethylamine, ChiPros 99+%, ee 99+%
CAS:(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 reagFórmula:C12H13NPureza:99+%Forma y color:White to pale yellow, Crystals or powder or crystalline powder or fused/lumpy solidPeso molecular:171.24(S)-(-)-1-(Naphthalen-2-yl)ethylamine
CAS:Fórmula:C12H13NPureza:97%Forma y color:SolidPeso molecular:171.2383(S)-(-)-1-(2-Naphthyl)ethylamine
CAS:(S)-(-)-1-(2-Naphthyl)ethylamineFórmula:C12H13NPureza:>98%Forma y color:SolidPeso molecular:171.23832(S)-1-(Naphthalen-2-yl)ethanamine
CAS:(S)-1-(Naphthalen-2-yl)ethanamineFórmula:C12H13NPureza:97%Peso molecular:171.24(S)-1-(Naphthalen-2-yl)ethanamine
CAS:Fórmula:C12H13NPureza:95%Forma y color:SolidPeso molecular:171.243(S)-1-(2-Naphthyl)ethylamine
CAS:(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.Fórmula:C12H13NPureza:Min. 95%Peso molecular:171.24 g/mol







