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13047-04-6 | 1,2-Benzenediol, 4-amino-
CAS No: 13047-04-6 Catalog No: AG000UHF MDL No:MFCD00939525
Product Description
Catalog Number:
AG000UHF
Chemical Name:
1,2-Benzenediol, 4-amino-
CAS Number:
13047-04-6
Molecular Formula:
C6H7NO2
Molecular Weight:
125.1253
MDL Number:
MFCD00939525
IUPAC Name:
4-aminobenzene-1,2-diol
InChI:
InChI=1S/C6H7NO2/c7-4-1-2-5(8)6(9)3-4/h1-3,8-9H,7H2
InChI Key:
KDHUXRBROABJBC-UHFFFAOYSA-N
SMILES:
Nc1ccc(c(c1)O)O
Properties
Complexity:
97.1
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:
1.2
Literature
| Title | Journal |
|---|---|
| Catechol-modified activated carbon prepared by the diazonium chemistry for application as active electrode material in electrochemical capacitor. | ACS applied materials & interfaces 20120801 |
| A cytokine mixture of GM-CSF and IL-3 that induces a neuroprotective phenotype of microglia leading to amelioration of (6-OHDA)-induced Parkinsonism of rats. | Brain and behavior 20110901 |
| Current approaches to the treatment of Parkinson's disease. | Neuropsychiatric disease and treatment 20080801 |
| Biotransformation of hydroxylaminobenzene and aminophenol by Pseudomonas putida 2NP8 cells grown in the presence of 3-nitrophenol. | Applied and environmental microbiology 20000601 |
| Identification of the aminocatechol A-3253 as an in vitro poison of DNA topoisomerase I from Candida albicans. | Antimicrobial agents and chemotherapy 19950301 |
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