What is the (R)-(+)-1-(1-Naphthyl)ethylamine?

(R)-(+)-1-(1-Naphthyl)ethylamine is Colorless to light yellow liquid, while it's Molecular Formula is C12H13N. Colorless to light yellow liquid It is used in chiral synthesis in organic reactions including the synthesis of β-amino acids and the enantioselective of ketones to nitroolefins. Also used as absolute configuration of primary amines determined using chiral (2-nitrophenyl)proline amides and H NMR.

What is the CAS number for (R)-(+)-1-(1-Naphthyl)ethylamine?

The CAS number of (R)-(+)-1-(1-Naphthyl)ethylamine is 3886-70-2.

What is the (R)-(+)-1-(1-Naphthyl)ethylamine?

(R)-(+)-1-(1-Naphthyl)ethylamine is Colorless to light yellow liquid, while it's Molecular Formula is C12H13N. Colorless to light yellow liquid It is used in chiral synthesis in organic reactions including the synthesis of β-amino acids and the enantioselective of ketones to nitroolefins. Also used as absolute configuration of primary amines determined using chiral (2-nitrophenyl)proline amides and H NMR.

What is the CAS number for (R)-(+)-1-(1-Naphthyl)ethylamine?

The CAS number of (R)-(+)-1-(1-Naphthyl)ethylamine is 3886-70-2.

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3886-70-2

Product Name：(R)-(+)-1-(1-Naphthyl)ethylamine
Molecular Formula：C₁₂H₁₃N
Purity：99%
Molecular Weight：171.242

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Product Details

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Molecular Formula:C12H13N
Molecular Weight:171.242
Appearance/Colour:Colorless to light yellow liquid
Vapor Pressure:0.00214mmHg at 25°C
Melting Point:135-136 °C
Refractive Index:n20/D 1.623(lit.)
Boiling Point:289.9 °C at 760 mmHg
PKA:9.26±0.40(Predicted)
Flash Point:144.3 °C
PSA：26.02000
Density:1.064 g/cm³
LogP:3.55980

(R)-(+)-1-(1-Naphthyl)ethylamine(Cas 3886-70-2) Usage

Chemical Properties	Colorless to light yellow liqui
Uses	(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.
General Description	(R)-(+)-1-(1-Naphthyl)ethylamine is a chiral derivatization reagent useful for all gas chromatography (GC) applications in the chiral field. It is specially selected to meet the requirements for derivatization reagents for enantiomeric excess determinations.

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

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3886-70-2 Process route

: 10420-89-0
(S)-1-(1-Naphthyl)ethylamine

: 100-41-4,27536-89-6
ethylbenzene

: 3886-70-2
(R)-1-(1-Naphthyl)ethylamine

Conditions

Conditions	Yield
With hydrogen; Pd-BaSO₄; In toluene; at 70 ℃; for 24h; under 75.0075 Torr;

: 42882-31-5
(RS)-1-(1-naphthyl)ethylamine

: 3886-70-2
(R)-1-(1-Naphthyl)ethylamine

Conditions

Conditions	Yield
With p-chlorophenyl pentanoate; hydrogen; In toluene; at 55 ℃; for 15h; under 75.0075 Torr; Enzymatic reaction;	88.3%
With D-(+)-camphoric acid;
Multi-step reaction with 3 steps 1: ethanol / 0.75 h / 60 - 65 °C / Resolution of racemate 2: ammonia / water; toluene 3: potassium hydroxide / dimethyl sulfoxide / 20 h / 150 - 160 °C With ammonia; potassium hydroxide; In ethanol; water; dimethyl sulfoxide; toluene;
Multi-step reaction with 2 steps 1: water; methanol / 10 h / 60 - 65 °C 2: sodium hydroxide / water; toluene / 0.5 h / 25 - 35 °C / pH 12.5 - 13.5 With sodium hydroxide; In methanol; water; toluene;

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