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Home > Indoles and Oxindole > 3289-82-5
3289-82-5 | 1H-Indole, 1-hydroxy-
CAS No: 3289-82-5 Catalog No: AG007ILC MDL No:
Product Description
Catalog Number:
AG007ILC
Chemical Name:
1H-Indole, 1-hydroxy-
CAS Number:
3289-82-5
Molecular Formula:
C8H7NO
Molecular Weight:
133.1473
IUPAC Name:
1-hydroxyindole
InChI:
InChI=1S/C8H7NO/c10-9-6-5-7-3-1-2-4-8(7)9/h1-6,10H
InChI Key:
PTXVSDKCUJCCLC-UHFFFAOYSA-N
SMILES:
On1ccc2c1cccc2
Properties
Complexity:
126
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
133.053g/mol
Formal Charge:
0
Heavy Atom Count:
10
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
133.15g/mol
Monoisotopic Mass:
133.053g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
25.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.8
Literature
| Title | Journal |
|---|---|
| The gramine route to pyrido[4,3-b]indol-3-ones - identification of a new cytotoxic lead. | Scientia pharmaceutica 20110101 |
| On the mechanism of nitrosoarene-alkyne cycloaddition. | Journal of the American Chemical Society 20090121 |
| [Imagination and creation: 1-hydroxyindole chemistry and the dream challenge]. | Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 20080401 |
| Dehydrogenation of indoline by cytochrome P450 enzymes: a novel 'aromatase' process. | The Journal of pharmacology and experimental therapeutics 20070801 |
| New indole N-oxide alkaloids from Evodia fargesii. | Planta medica 20060201 |
| Birnbaumin A and B: two unusual 1-hydroxyindole pigments from the 'flower pot parasol' Leucocoprinus birnbaumii. | Angewandte Chemie (International ed. in English) 20050506 |
| A new antibiotic CJ-17,665 from Aspergillus ochraceus. | The Journal of antibiotics 20011101 |
| The chemistry of indoles. CIII. Simple syntheses of serotonin, N-methylserotonin, bufotenine, 5-methoxy-N-methyltryptamine, bufobutanoic acid, N-(indol-3-yl)methyl-5-methoxy-N-methyltryptamine, and lespedamine based on 1-hydroxyindole chemistry. | Chemical & pharmaceutical bulletin 20010101 |
| O-glycosides of N-hydroxyindoles. | Nucleosides, nucleotides & nucleic acids 20010101 |
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