Home Amines 23364-44-5
23364-44-5,MFCD00074959
Catalog No.:AA002MX5

23364-44-5 | (1S,2R)-(+)-2-Amino-1,2-diphenylethanol

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1g
>98%(GC)
in stock  
$24.00   $17.00
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5g
98%
in stock  
$29.00   $20.00
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25g
98%
in stock  
$49.00   $34.00
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100g
98%
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$147.00   $103.00
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500g
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$685.00   $480.00
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  • Technical Information
  • Properties
  • Literature
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  • Download SDS
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA002MX5
Chemical Name:
(1S,2R)-(+)-2-Amino-1,2-diphenylethanol
CAS Number:
23364-44-5
Molecular Formula:
C14H15NO
Molecular Weight:
213.2750
MDL Number:
MFCD00074959
SMILES:
N[C@@H]([C@H](c1ccccc1)O)c1ccccc1
Properties
Properties
 
BP:
374.3°C at 760 mmHg  
Form:
Solid  
MP:
142-144 C  
Refractive Index:
7 ° (C=0.6, EtOH)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
195  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
3  
XLogP3:
1.3  

Literature

Title: Synthesis of dendrimer-type chiral stationary phases based on the selector of (1S,2R)-(+)-2-amino-1,2-diphenylethanol derivate and their enantioseparation evaluation by HPLC.

Journal: Chirality 20100101

Title: NMDA receptor affinities of 1,2-diphenylethylamine and 1-(1,2-diphenylethyl)piperidine enantiomers and of related compounds.

Journal: Bioorganic & medicinal chemistry 20090501

Title: Immobilization of (1S,2R)-(+)-2-amino-1,2-diphenylethanol derivates on aminated silica gel with different linkages as chiral stationary phases and their enantioseparation evaluation by HPLC.

Journal: Chirality 20090401

Title: Asymmetric synthesis of [2,3-(13)C(2),(15)N]-4-benzyloxy-5,6-diphenyl-2,3,5,6-tetrahydro-4H-oxazine-2-one via lipase TL-mediated kinetic resolution of benzoin: general procedure for the synthesis of [2,3-(13)C(2),(15)N]-L-alanine.

Journal: The Journal of organic chemistry 20011130

Title: Solid-phase synthesis of homogeneous ruthenium catalysts on silica for the continuous asymmetric transfer hydrogenation reaction.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20010316

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SDS
Tags:23364-44-5 Molecular Formula|23364-44-5 MDL|23364-44-5 SMILES|23364-44-5 (1S,2R)-(+)-2-Amino-1,2-diphenylethanol |Organic_Building_Blocks