Home Other Building Blocks 4-Amino-3-hydroxybenzoic acid

4-Amino-3-hydroxybenzoic acid

CAS No.:
2374-03-0
Catalog Number:
AG0033WC
Molecular Formula:
C7H7NO3
Molecular Weight:
153.1354
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
97%
In Stock USA
United States
$13
- +
5g
97%
In Stock USA
United States
$19
- +
25g
97%
In Stock USA
United States
$75
- +
100g
97%
In Stock USA
United States
$225
- +
500g
97%
In Stock USA
United States
$850
- +
Product Description
Catalog Number:
AG0033WC
Chemical Name:
4-Amino-3-hydroxybenzoic acid
CAS Number:
2374-03-0
Molecular Formula:
C7H7NO3
Molecular Weight:
153.1354
MDL Number:
MFCD00017094
IUPAC Name:
4-amino-3-hydroxybenzoic acid
InChI:
InChI=1S/C7H7NO3/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3,9H,8H2,(H,10,11)
InChI Key:
NFPYJDZQOKCYIE-UHFFFAOYSA-N
SMILES:
OC(=O)c1ccc(c(c1)O)N
EC Number:
629-073-2
NSC Number:
407243
Properties
Complexity:
160  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
153.043g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
153.137g/mol
Monoisotopic Mass:
153.043g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
83.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.8  
Literature
Title Journal
Redox potentials, laccase oxidation, and antilarval activities of substituted phenols. Bioorganic & medicinal chemistry 20120301
A copper-containing oxidase catalyzes C-nitrosation in nitrosobenzamide biosynthesis. Nature chemical biology 20100901
Gene cloning and characterization of a deaminase from the 4-amino-3-hydroxybenzoate-assimilating Bordetella sp. strain 10d. FEMS microbiology letters 20090901
3D-QSAR and molecular docking studies of benzaldehyde thiosemicarbazone, benzaldehyde, benzoic acid, and their derivatives as phenoloxidase inhibitors. Bioorganic & medicinal chemistry 20070301
Metabolism of 4-amino-3-hydroxybenzoic acid by Bordetella sp. strain 10d: A different modified meta-cleavage pathway for 2-aminophenols. Bioscience, biotechnology, and biochemistry 20061101
Interaction of mushroom tyrosinase with aromatic amines, o-diamines and o-aminophenols. Biochimica et biophysica acta 20040804
A novel coupled enzyme assay reveals an enzyme responsible for the deamination of a chemically unstable intermediate in the metabolic pathway of 4-amino-3-hydroxybenzoic acid in Bordetella sp. strain 10d. European journal of biochemistry 20040801
Cloning of a gene encoding 4-amino-3-hydroxybenzoate 2,3-dioxygenase from Bordetella sp. 10d. Biochemical and biophysical research communications 20040206
A novel meta-cleavage dioxygenase that cleaves a carboxyl-group-substituted 2-aminophenol. Purification and characterization of 4-amino-3-hydroxybenzoate 2,3-dioxygenase from Bordetella sp. strain 10d. European journal of biochemistry 20021201
Properties