3163-15-3 | 2-Aminoresorcinol

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$15.00	$10.00
1g	97%	in stock	$18.00	$12.00
5g	97%	in stock	$40.00	$28.00
10g	97%	in stock	$79.00	$55.00
25g	97%	in stock	$196.00	$137.00
100g	97%	in stock	$782.00	$547.00
500g	97%	in stock	$3,401.00	$2,381.00

Description

• Catalog Number: AB61229
• Chemical Name: 2-Aminoresorcinol
• CAS Number: 3163-15-3
• Molecular Formula: C6H7NO2
• Molecular Weight: 125.1253
• MDL Number: MFCD00128992
• SMILES: Oc1cccc(c1N)O

Computed Properties

• Complexity: 87.1
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 3
• XLogP3: 0.5

Literature

• Synthesis and the intestinal glucosidase inhibitory activity of 2-aminoresorcinol derivatives toward an investigation of its binding site.

  Bioscience, biotechnology, and biochemistry 20120101

• Detection of the reaction intermediates catalyzed by a copper amine oxidase.

  Journal of synchrotron radiation 20110101

• 2-Aminoresorcinol is a potent alpha-glucosidase inhibitor.

  Bioorganic & medicinal chemistry letters 20080115

• Environmentally friendly chemoselective oxidation of primary aliphatic amines by using a biomimetic electrocatalytic system.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20080101

• Decolorization and partial degradation of monoazo dyes in sequential fixed-film anaerobic batch reactor (SFABR).

  Bioresource technology 20070701

• Electrochemically induced cascade reaction for the assembly of libraries of biologically relevant 1,4-benzoxazine derivatives.

  The Journal of organic chemistry 20060818

• Mechanism-based cofactor derivatization of a copper amine oxidase by a branched primary amine recruits the oxidase activity of the enzyme to turn inactivator into substrate.

  Journal of the American Chemical Society 20060510

• A convenient approach for evaluating the toxicity profiles of in vitro neuroprotective alkylaminophenol derivatives.

  Free radical biology & medicine 20060301

• Anti-Plasmodium activity of ceramide analogs.

  Malaria journal 20040101

• Role of copper ion in bacterial copper amine oxidase: spectroscopic and crystallographic studies of metal-substituted enzymes.

  Journal of the American Chemical Society 20030129

• Spectroscopic observation of intermediates formed during the oxidative half-reaction of copper/topa quinone-containing phenylethylamine oxidase.

  Biochemistry 20011225