3886-70-2
- Product Name:(R)-(+)-1-(1-Naphthyl)ethylamine
 - Molecular Formula:C12H13N
 - Purity:99%
 - Molecular Weight:171.242
 
Product Details
Quality Factory Supply Hot Sale (R)-(+)-1-(1-Naphthyl)ethylamine 3886-70-2 with Safe Transportation
- 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
3886-70-2 Relevant articles
A METHOD FOR PREPARATION OF DIASTEREOMERIC LACTATE SALTS OF 1-(1-NAPHTHYL)ETHYL AMINE AND PURE ENANTIOMERS OF 1-(1-NAPHTHYL)ETHYL AMINE
-
Paragraph 0048, (2021/09/11)
The invention relates to method for prep...
Asymmetric reduction method of nitrogen-phosphonyl protected imine
-
Paragraph 0180-0185, (2021/01/15)
The invention discloses an asymmetric re...
Enzymatic Primary Amination of Benzylic and Allylic C(sp3)-H Bonds
Jia, Zhi-Jun,Gao, Shilong,Arnold, Frances H.
supporting information, p. 10279 - 10283 (2020/07/27)
Aliphatic primary amines are prevalent i...
Addition of Highly Polarized Organometallic Compounds to N-tert-Butanesulfinyl Imines in Deep Eutectic Solvents under Air: Preparation of Chiral Amines of Pharmaceutical Interest
Capriati, Vito,Cicco, Luciana,García-álvarez, Joaquín,González-Sabín, Javier,Perna, Filippo M.,Ríos-Lombardía, Nicolás,Salomone, Antonio,Vitale, Paola
, (2020/07/04)
Highly polarized organometallic compound...
3886-70-2 Process route
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 - 10420-89-0
	
(S)-1-(1-Naphthyl)ethylamine
 

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

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 - 3886-70-2
	
(R)-1-(1-Naphthyl)ethylamine
 
| 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 | 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;    
			 | 
			
3886-70-2 Upstream products
- 
	42882-31-5

(RS)-1-(1-naphthyl)ethylamine
 - 
	371-27-7

2,2,2-trifluoroethylbutyrate
 - 
	121328-40-3

(S)-4-Isopropyl-3-((R)-1-naphthalen-1-yl-ethyl)-oxazolidin-2-one
 - 
	74629-94-0

(1S,2R,R)-cis-1-(2-Hydroxy-1,2,3,4-tetrahydro-1-naphthyl)methyl N-<1-(1-naphthyl)ethyl>amide
 
3886-70-2 Downstream products
- 
	64187-98-0

(1R,2'S)-N-<1-(1-naphthyl)ethyl>-2-phenylbutanamide
 - 
	72165-50-5

(R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid 3-hydroxy-3-methyl-4-((R)-1-naphthalen-1-yl-ethylcarbamoyl)-butyl ester
 - 
	77732-38-8

(3S,1'R)-N-(1-naphthylethyl)-3-(4-methylphenyl)butanamide
 - 
	77732-39-9

(3R,1'R)-N-(1-naphthylethyl)-3-(4-methylphenyl)butanamide
 
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