Home Other Building Blocks (S)-2-Amino-1-phenylethanol

(S)-2-Amino-1-phenylethanol

CAS No.:
56613-81-1
Catalog Number:
AG003CDS
Molecular Formula:
C8H11NO
Molecular Weight:
137.1790
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$25
- +
5g
98%
In Stock USA
United States
$81
- +
10g
98%
In Stock USA
United States
$150
- +
25g
98%
In Stock USA
United States
$338
- +
Product Description
Catalog Number:
AG003CDS
Chemical Name:
(S)-2-Amino-1-phenylethanol
CAS Number:
56613-81-1
Molecular Formula:
C8H11NO
Molecular Weight:
137.1790
MDL Number:
MFCD00239405
IUPAC Name:
(1S)-2-amino-1-phenylethanol
InChI:
InChI=1S/C8H11NO/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8,10H,6,9H2/t8-/m1/s1
InChI Key:
ULSIYEODSMZIPX-MRVPVSSYSA-N
SMILES:
NC[C@H](c1ccccc1)O
Properties
Complexity:
89.3  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
137.084g/mol
Formal Charge:
0
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
137.182g/mol
Monoisotopic Mass:
137.084g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
46.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.1  
Literature
Title Journal
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. Organic & biomolecular chemistry 20110221
Enantioselective gel collapsing: a new means of visual chiral sensing. Journal of the American Chemical Society 20100602
Asymmetric synthesis of 8-aminoindolizidine from chiral 2-pyrroleimines. The Journal of organic chemistry 20081107
Formal total synthesis of (+)-gephyrotoxin. The Journal of organic chemistry 20080815
Enantioseparation of phenylglycinol in chiral-modified zeolite HY: a molecular simulation study. Chirality 20070601
Practical enantioselective synthesis of beta-substituted-beta-amino esters. The Journal of organic chemistry 20050708
Stereoselective addition of dimethyl thiophosphite to imines. The Journal of organic chemistry 20040402
Molecular recognition of sub-micromolar inhibitors by the epinephrine-synthesizing enzyme phenylethanolamine N-methyltransferase. Journal of medicinal chemistry 20040101
Employing the structural diversity of nature: development of modular dipeptide-analogue ligands for ruthenium-catalyzed enantioselective transfer hydrogenation of ketones. Chemistry (Weinheim an der Bergstrasse, Germany) 20030905
Phenylethanolamine N-methyltransferase kinetics: bovine versus recombinant human enzyme. Bioorganic & medicinal chemistry letters 20010618
Enantioselective syntheses of dopaminergic (R)- and (S)-benzyltetrahydroisoquinolines. Journal of medicinal chemistry 20010524
Properties