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56210-72-1

  • Product Name(-)-Bis[(S)-1-phenylethyl]amine
  • Molecular FormulaC16H19 N
  • Molecular Weight225.334
  • Purity99%
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Product Details

Quick Details

  • CasNo: 56210-72-1
  • Molecular Formula: C16H19 N
  • Purity: 99%

Buy high quality and low price (-)-Bis[(S)-1-phenylethyl]amine 56210-72-1 now

  • Molecular Formula:C16H19N
  • Molecular Weight:225.334
  • Vapor Pressure:0.00143mmHg at 25°C 
  • Melting Point:~260 °C
     
  • Refractive Index:n20/D 1.5525(lit.) 
  • Boiling Point:86 ºC (0.05 mmHg) 
  • PKA:8.79±0.29(Predicted) 
  • Flash Point:113 ºC 
  • PSA:12.03000 
  • Density:0.987 
  • LogP:4.48930 

(-)-Bis[(S)-1-phenylethyl]amine(Cas 56210-72-1) Usage

InChI:InChI=1/C16H19N/c1-13(15-9-5-3-6-10-15)17-14(2)16-11-7-4-8-12-16/h3-14,17H,1-2H3/t13-,14-/m0/s1

56210-72-1 Relevant articles

An Iridium Catalytic System Compatible with Inorganic and Organic Nitrogen Sources for Dual Asymmetric Reductive Amination Reactions

Chang, Mingxin,Gao, Zhaofeng,Geng, Huiling,Huang, Haizhou,Liu, Jingwen

supporting information, p. 27307 - 27311 (2021/11/17)

Asymmetric reductive amination (ARA) is ...

Method for synthesizing chiral phosphite ligand based on R - 2 - phenylethylamine

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Paragraph 0011; 0040; 0046, (2021/10/27)

The invention discloses a method for syn...

One-Pot Synthesis of Symmetrical Tertiary and Secondary Amines from Carbonyl Compounds, Ammonium Carbonate and Carbon Monoxide as a Reductant

Muratov, Karim,Afanasyev, Oleg I.,Kuchuk, Ekaterina,Runikhina, Sofiya,Chusov, Denis

supporting information, p. 6557 - 6560 (2019/10/22)

Rh-catalyzed one-step synthesis of terti...

Preparation method of chiral amine compounds

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Paragraph 0018, (2018/09/13)

The invention discloses a preparation me...

56210-72-1 Process route

(<i>S</i>)-1-phenyl-ethylamine
2627-86-3

(S)-1-phenyl-ethylamine

acetophenone
98-86-2

acetophenone

1-Phenylethanol
98-85-1,13323-81-4

1-Phenylethanol

(1S,1'S)-bis(1-phenylethyl)amine
21003-56-5,21003-57-6,23294-41-9,42287-48-9,56210-72-1,10024-74-5

(1S,1'S)-bis(1-phenylethyl)amine

Conditions
Conditions Yield
(S)-1-phenyl-ethylamine; acetophenone; With tris(pentafluorophenyl)borate; In toluene; at 60 ℃; for 8h;
With ammonia borane; In toluene; at 60 ℃; for 4h; Solvent; Temperature; diastereoselective reaction;
37%
53%
acetophenone
98-86-2

acetophenone

(<i>S</i>)-1-phenyl-ethylamine
2627-86-3

(S)-1-phenyl-ethylamine

(R)-1-phenyl-ethyl-amine
3886-69-9

(R)-1-phenyl-ethyl-amine

(1S,1'S)-bis(1-phenylethyl)amine
21003-56-5,21003-57-6,23294-41-9,42287-48-9,56210-72-1,10024-74-5

(1S,1'S)-bis(1-phenylethyl)amine

(R,R)-N,N-bis-(1-phenylethyl)amine
10024-74-5,21003-56-5,21003-57-6,23294-41-9,42287-48-9,56210-72-1

(R,R)-N,N-bis-(1-phenylethyl)amine

(R,S)-bis(1-phenylethyl)amine
21003-57-6,1163726-07-5

(R,S)-bis(1-phenylethyl)amine

Conditions
Conditions Yield
With bis(1,5-cyclooctadiene)diiridium(I) dichloride; (R)-1-[(SP)-2-(diphenylphosphino)ferrocenyl]ethyl-di-tert-butylphosphine; ammonium acetate; hydrogen; toluene-4-sulfonic acid; In methanol; dichloromethane; at 80 ℃; for 24h; under 45603.1 Torr; stereoselective reaction; Autoclave;
4 % ee
12 % ee
With bis(1,5-cyclooctadiene)diiridium(I) dichloride; C37H30NO2P; ammonium acetate; hydrogen; toluene-4-sulfonic acid; In methanol; dichloromethane; at 80 ℃; for 24h; under 45603.1 Torr; Reagent/catalyst; stereoselective reaction; Autoclave;
26 % ee
6 % ee
With bis(1,5-cyclooctadiene)diiridium(I) dichloride; ammonium acetate; hydrogen; C45H34NO2P; toluene-4-sulfonic acid; In methanol; dichloromethane; at 80 ℃; for 24h; under 45603.1 Torr; Reagent/catalyst; stereoselective reaction; Autoclave;
66 % ee
18 % ee

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56210-72-1 Downstream products

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  • 134431-03-1
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    benzyl (3R,αR,α'R)-3-(N,N-bis(α-methylbenzyl)amino)butanoate

  • 137219-70-6
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    2-{[Bis-((S)-1-phenyl-ethyl)-amino]-methyl}-acrylic acid tert-butyl ester

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