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4-Hydroxybenzonitrile, 98+%, Thermo Scientific Chemicals
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Catalog number A15803.30
also known as A15803-30
Price (USD)/ Each
293.00
-
Quantity:
250 g
Price (USD)/ Each
293.00
4-Hydroxybenzonitrile, 98+%, Thermo Scientific Chemicals
Catalog numberA15803.30
Price (USD)/ Each
293.00
-
Chemical Identifiers
CAS767-00-0
IUPAC Name4-hydroxybenzonitrile
Molecular FormulaC7H5NO
InChI KeyCVNOWLNNPYYEOH-UHFFFAOYSA-N
SMILESOC1=CC=C(C=C1)C#N
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to cream
FormPowder
Melting Point (clear melt)110-115?C
Assay (GC)≥98.0%
4-Hydroxybenzonitrile is used as an intermediate in organic synthesis. It is also used in cosmetic as an antiseptic and disinfectant. It is involved as a raw material for the preparation of bomoxynil and ioxynil.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
4-Hydroxybenzonitrile is used as an intermediate in organic synthesis. It is also used in cosmetic as an antiseptic and disinfectant. It is involved as a raw material for the preparation of bomoxynil and ioxynil.
Solubility
Soluble in methanol. Insoluble in water.
Notes
Incompatible with strong oxidizing agents.
4-Hydroxybenzonitrile is used as an intermediate in organic synthesis. It is also used in cosmetic as an antiseptic and disinfectant. It is involved as a raw material for the preparation of bomoxynil and ioxynil.
Solubility
Soluble in methanol. Insoluble in water.
Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Durgannavar, A. K.; Patgar, M. B.; Chimatadar, S. A. Oxidation of amoxicillin by hexacyanoferrate(III) in aqueous alkaline medium-A kinetic and mechanistic approach. Indian J Chem 2015, 54 (9), 1085-1091.
- Zhang, J.; Wu, W.; Ji, X.; Cao, S. Perfluorobutyl iodide-assisted direct cyanomethylation of azoles and phenols with acetonitrile. RSC Adv. 2015, 5 (26), 20562-20565.