Home Other Building Blocks 2-Aminoresorcinol

2-Aminoresorcinol

CAS No.:
3163-15-3
Catalog Number:
AG003GK5
Molecular Formula:
C6H7NO2
Molecular Weight:
125.1253
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
97%
In Stock USA
United States
$35
- +
5g
97%
In Stock USA
United States
$110
- +
10g
97%
In Stock USA
United States
$198
- +
25g
97%
In Stock USA
United States
$398
- +
100g
97%
In Stock USA
United States
$1038
- +
Product Description
Catalog Number:
AG003GK5
Chemical Name:
2-Aminoresorcinol
CAS Number:
3163-15-3
Molecular Formula:
C6H7NO2
Molecular Weight:
125.1253
MDL Number:
MFCD00128992
IUPAC Name:
2-aminobenzene-1,3-diol
InChI:
InChI=1S/C6H7NO2/c7-6-4(8)2-1-3-5(6)9/h1-3,8-9H,7H2
InChI Key:
JEPCLNGRAIMPQV-UHFFFAOYSA-N
SMILES:
Oc1cccc(c1N)O
EC Number:
926-781-6
Properties
Complexity:
87.1  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
125.048g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
125.127g/mol
Monoisotopic Mass:
125.048g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
66.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.5  
Literature
Title Journal
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
Properties