55-81-2 | 2-(4-Methoxyphenyl)ethylamine

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$25.00	$18.00
5g	98%	in stock	$66.00	$47.00
25g	98%	in stock	$139.00	$97.00
100g	98%	in stock	$356.00	$249.00
500g	98%	in stock	$1,319.00	$923.00

Description

• Catalog Number: AB67851
• Chemical Name: 2-(4-Methoxyphenyl)ethylamine
• CAS Number: 55-81-2
• Molecular Formula: C9H13NO
• Molecular Weight: 151.2056
• MDL Number: MFCD00008192
• SMILES: NCCc1ccc(cc1)OC
• NSC Number: 43687

Computed Properties

• Complexity: 97.7
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 1.6

Literature

• Next generation techniques in the high resolution spectroscopy of biologically relevant molecules.

  Physical chemistry chemical physics : PCCP 20110428

• 4-(4-Meth-oxy-pheneth-yl)-3-methyl-1H-1,2,4-triazol-5(4H)-one.

  Acta crystallographica. Section E, Structure reports online 20100801

• Human and mouse trace amine-associated receptor 1 have distinct pharmacology towards endogenous monoamines and imidazoline receptor ligands.

  The Biochemical journal 20091023

• Structure-activity correlations for beta-phenethylamines at human trace amine receptor 1.

  Bioorganic & medicinal chemistry 20080801

• Electrochemical Investigation of oligonucleotide-DNA hybridization on poly(4-methoxyphenethylamine).

  International journal of molecular sciences 20080601

• Synthesis and 3D QSAR of new pyrazolo[3,4-b]pyridines: potent and selective inhibitors of A1 adenosine receptors.

  Journal of medicinal chemistry 20051117

• Inhibition of lentil copper/TPQ amine oxidase by the mechanism-based inhibitor derived from tyramine.

  Biological chemistry 20040101

• Regioselective enzyme-catalyzed synthesis of sophorolipid esters, amides, and multifunctional monomers.

  The Journal of organic chemistry 20030711

• Role of glutamic acid 216 in cytochrome P450 2D6 substrate binding and catalysis.

  Biochemistry 20030211

• Oxidation of methoxyphenethylamines by cytochrome P450 2D6. Analysis of rate-limiting steps.

  The Journal of biological chemistry 20020913

• Oxidation of phenethylamine derivatives by cytochrome P450 2D6: the issue of substrate protonation in binding and catalysis.

  Biochemistry 20011127