2-Amino-1-phenylethanol - CAS 7568-93-6

Catalog:	BB035374
Product Name:	2-Amino-1-phenylethanol
CAS:	7568-93-6
Synonyms:	2-amino-1-phenylethanol

Technical Data

Safety and Hazards

Patents

Literatures

Computed Properties

IUPAC Name:	2-amino-1-phenylethanol
Description:	2-Amino-1-phenylethanol (CAS# 7568-93-6) is used as topical vasoconstrictor.
Molecular Weight:	137.18
Molecular Formula:	C8H11NO
Canonical SMILES:	C1=CC=C(C=C1)C(CN)O
InChI:	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
Boiling Point:	160 °C at 17 mmHg
Melting Point:	56.5 °C
Purity:	96 %
Solubility:	45.8 mg/mL
Appearance:	White solid
MDL:	MFCD00008137
LogP:	1.37900
Vapor Pressure:	0.00132 [mmHg]

Publication Number	Title	Priority Date
CN-113512545-A	Immobilized lipase synthesis and new method for splitting mandelic acid enantiomer	20210727
CN-113414344-A	Self-hardening furan resin for low-moisture casting and preparation method thereof	20210623
CN-113046026-A	Chlorine-free low-corrosivity coal antifreezing solution	20210407
CN-112877072-A	Long-acting agriculture and forestry water-retaining agent and preparation method thereof	20210114
CN-112845279-A	Environment-friendly energy-saving novel metal cold forming processing method	20201224

PMID	Publication Date	Title	Journal
30643208	20190801	Discovery of β-arrestin-biased β2-adrenoceptor agonists from 2-amino-2-phenylethanol derivatives	Acta pharmacologica Sinica
22411183	20120701	A simple and sensitive method for the demonstration of norepinephrine-storing adrenomedullary chromaffin cells	Histochemistry and cell biology
22665130	20120701	Endothelial cells are able to synthesize and release catecholamines both in vitro and in vivo	Hypertension (Dallas, Tex. : 1979)
22717559	20120701	Determination of phenylethanolamine A in animal hair, tissues and feeds by reversed phase liquid chromatography tandem mass spectrometry with QuEChERS	Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
22738036	20120627	Differential effects of Mycobacterium bovis--derived polar and apolar lipid fractions on bovine innate immune cells	Veterinary research

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Related Functional Groups

Alcohols and Derivatives

[58287-18-6]
(1R)-1-(4-Nitrophenyl)ethanol
[77987-49-6]
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[64437-48-5]
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[112256-09-4]
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[1183749-69-0]
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Oxygen Compounds

[544-62-7]
Batyl alcohol
[1427004-19-0]
DBCO-PEG4-NHS ester
[77987-49-6]
Z-Glycinol
[5896-75-3]
(Z)-N-(4-Phenylpiperazin-1-yl)-1-(2,3,4-trimethoxyphenyl)methanimine
[1035840-45-9]
1-(5-Methoxy-1,3-benzoxazol-2-yl)piperidine-3-carboxylic acid
[1006443-01-1]
1-(5-Nitropyridin-2-yl)-1H-pyrazole-3-carboxylic acid

GHS Hazard Statement:	H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
Precautionary Statement:	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word:	Warning

Complexity:	89.3
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	137.084063974
Formal Charge:	0
Heavy Atom Count:	10
Hydrogen Bond Acceptor Count:	2
Hydrogen Bond Donor Count:	2
Isotope Atom Count:	0
Monoisotopic Mass:	137.084063974
Rotatable Bond Count:	2
Topological Polar Surface Area:	46.2 Å²
Undefined Atom Stereocenter Count:	1
Undefined Bond Stereocenter Count:	0
XLogP3:	0.1