Home Amines 56613-81-1
56613-81-1,MFCD00239405
Catalog No.:AA003CB0

56613-81-1 | (S)-2-Amino-1-phenylethanol

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1g
97%
in stock  
$37.00   $26.00
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5g
95%
in stock  
$66.00   $47.00
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10g
95%
in stock  
$117.00   $82.00
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25g
97%
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$225.00   $157.00
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100g
97%
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$863.00   $604.00
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  • Technical Information
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  • Technical Information
  • Properties
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Technical Information
Catalog Number:
AA003CB0
Chemical Name:
(S)-2-Amino-1-phenylethanol
CAS Number:
56613-81-1
Molecular Formula:
C8H11NO
Molecular Weight:
137.1790
MDL Number:
MFCD00239405
SMILES:
NC[C@H](c1ccccc1)O
Properties
Properties
 
BP:
283.5 °C at 760 mmHg  
Form:
Solid  
MP:
57-59°C  
Solubility:
Soluble in methanol.  
Stability:
Air Sensitive  
Storage:
Light sensitive;Inert atmosphere;-20 ℃;  

Computed Properties
 
Complexity:
89.3  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
2  
XLogP3:
0.1  

Literature

Title: On the enantioselectivity of aziridination of styrene catalysed by copper triflate and copper-exchanged zeolite Y: consequences of the phase behaviour of enantiomeric mixtures of N-arene-sulfonyl-2-phenylaziridines.

Journal: Organic & biomolecular chemistry 20110221

Title: Enantioselective gel collapsing: a new means of visual chiral sensing.

Journal: Journal of the American Chemical Society 20100602

Title: Asymmetric synthesis of 8-aminoindolizidine from chiral 2-pyrroleimines.

Journal: The Journal of organic chemistry 20081107

Title: Formal total synthesis of (+)-gephyrotoxin.

Journal: The Journal of organic chemistry 20080815

Title: Enantioseparation of phenylglycinol in chiral-modified zeolite HY: a molecular simulation study.

Journal: Chirality 20070601

Title: Practical enantioselective synthesis of beta-substituted-beta-amino esters.

Journal: The Journal of organic chemistry 20050708

Title: Stereoselective addition of dimethyl thiophosphite to imines.

Journal: The Journal of organic chemistry 20040402

Title: Molecular recognition of sub-micromolar inhibitors by the epinephrine-synthesizing enzyme phenylethanolamine N-methyltransferase.

Journal: Journal of medicinal chemistry 20040101

Title: Employing the structural diversity of nature: development of modular dipeptide-analogue ligands for ruthenium-catalyzed enantioselective transfer hydrogenation of ketones.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20030905

Title: Phenylethanolamine N-methyltransferase kinetics: bovine versus recombinant human enzyme.

Journal: Bioorganic & medicinal chemistry letters 20010618

Title: Enantioselective syntheses of dopaminergic (R)- and (S)-benzyltetrahydroisoquinolines.

Journal: Journal of medicinal chemistry 20010524

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SDS
Tags:56613-81-1 Molecular Formula|56613-81-1 MDL|56613-81-1 SMILES|56613-81-1 (S)-2-Amino-1-phenylethanol |Organic_Building_Blocks