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A72405

Sigma-Aldrich

2-Amino-1-phenylethanol

98%

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Synonym(s):
α-(Aminomethyl)benzyl alcohol, DL-β-Hydroxyphenethylamine, Phenylethanolamine
Linear Formula:
NH2CH2CH(OH)C6H5
CAS Number:
7568-93-6
Molecular Weight:
137.18
Beilstein/REAXYS Number:
971222
EC Number:
231-469-1
MDL number:
MFCD00008137
UNSPSC Code:
12352100
PubChem Substance ID:
24891194
NACRES:
NA.22

Quality Level

100

assay

98%

form

solid

bp

160 °C/17 mmHg (lit.)

mp

56-58 °C (lit.)

SMILES string

NCC(O)c1ccccc1

InChI

1S/C8H11NO/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8,10H,6,9H2

InChI key

ULSIYEODSMZIPX-UHFFFAOYSA-N

Gene Information

human ... PNMT(5409)

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Sigma-Aldrich

190438

(S)-(−)-2-Amino-3-phenyl-1-propanol

Qian Wu et al.
Journal of medicinal chemistry, 48(23), 7243-7252 (2005-11-11)
The X-ray structure of human phenylethanolamine N-methyltransferase (hPNMT) complexed with its product, S-adenosyl-L-homocysteine (4), and the most potent inhibitor reported to date, SK&F 64139 (7), was used to identify the residues involved in inhibitor binding. Four of these residues, Val53
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M Weinstock et al.
Neuropharmacology, 43(6), 999-1005 (2002-11-09)
TV-3326 is a novel cholinesterase inhibitor that produces irreversible brain-selective inhibition of monoamine oxidase (MAO)-A and B and has antidepressant-like activity in rats after chronic oral administration. This study determined whether TV-3326 would cause less potentiation than other irreversible MAO-inhibitors
Panayiotis A Procopiou et al.
Journal of medicinal chemistry, 52(8), 2280-2288 (2009-03-26)
A series of saligenin alkoxyalkylphenylsulfonamide beta(2) adrenoceptor agonists were prepared by reacting a protected saligenin oxazolidinone with alkynyloxyalkyl bromides, followed by Sonogashira reaction, hydrogenation, and deprotection. The meta-substituted primary sulfonamide was more potent than the para- and the ortho-analogues. Primary
Masashi Imanishi et al.
Journal of medicinal chemistry, 51(15), 4804-4822 (2008-07-25)
We designed a series of benzoic acid derivatives containing the biphenyl ether or biphenyl template on the RHS and a phenylethanolaminotetraline (PEAT) skeleton, which was prepared by highly stereoselective synthesis, to generate two structurally different lead compounds ( 10c, 10m)
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