Weight | 119.123 g/mol |
---|---|
Formula | C7H5NO |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
4-Hydroxybenzonitrile (767-00-0)
4-cyanophenol · 4-hydroxycyanobenzene
Score:
#2031 in Physics
,
#4941 in Biology
,
#6331 in Chemistry
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- Studies with 3,5-diiodo-4-hydroxybenzonitrile (ioxynil) and related compounds in soils and plants (Annals of Applied Biology, 1967)
- Dehalogenation of the Herbicides Bromoxynil (3,5-Dibromo-4-Hydroxybenzonitrile) and Ioxynil (3,5-Diiodino-4-Hydroxybenzonitrile) by Desulfitobacterium chlororespirans (Applied and Environmental Microbiology, 2005)
- Biodegradation of the herbicide bromoxynil (3,5-dibromo-4-hydroxybenzonitrile) by purified pentachlorophenol hydroxylase and whole cells of Flavobacterium sp. strain ATCC 39723 is accompanied by cyanogenesis. (Applied and Environmental Microbiology, 1992)
- Ab initio MO and experimental studies on the vibrational spectra and structure of 4-hydroxybenzonitrile and of its anion (Journal of Molecular Structure-theochem, 2001)
- Hydrogen-bonded liquid crystals from alkoxystilbazoles and 3-cyanophenols : structural control of mesomorphism. Molecular structure of the complex between 4-cyanophenol and 4-octyloxystilbazole (Journal of Materials Chemistry, 1995)
- Proton-Coupled Electron Transfer between 4-Cyanophenol and Photoexcited Rhenium(I) Complexes with Different Protonatable Sites (Inorganic Chemistry, 2012)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4-cyanophenol
- 4-hydroxycyanobenzene
-
SMILESC1=CC(=CC=C1C#N)O
-
InChIKeyCVNOWLNNPYYEOH-UHFFFAOYSA-N
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