C94009
4-Cyanophenol
95%
Synonym(s):
4-Hydroxybenzonitrile
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All Photos(3)
About This Item
Linear Formula:
NCC6H4OH
CAS Number:
Molecular Weight:
119.12
Beilstein:
386130
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
95%
form
crystals
mp
110-113 °C (lit.)
SMILES string
Oc1ccc(cc1)C#N
InChI
1S/C7H5NO/c8-5-6-1-3-7(9)4-2-6/h1-4,9H
InChI key
CVNOWLNNPYYEOH-UHFFFAOYSA-N
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Application
4-Cyanophenol is a precursor for the synthesis of a vasodilator, Levcromakalim. Bromination of 4-cyanophenol results in bromoxynil, a commercial herbicide. It can also be used as a component of deep eutectic solvent (DES) mixture.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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J E Harrison et al.
Pharmaceutical research, 13(4), 542-546 (1996-04-01)
The purpose of this work was to analyse the mechanism of the enhancement of percutaneous penetration demonstrated by the known enhancers Azone and Transcutol. Enhancer induced changes in the diffusivity and solubility of a model permeant (4-cyanophenol) in human stratum
A L Stinchcomb et al.
Pharmaceutical research, 16(8), 1288-1293 (1999-09-01)
Simple, safe and quick in vivo methods for estimating chemical uptake into the stratum corneum (SC) from volatile and non-volatile solvents are invaluable to health risk assessors. This study compares the human in vivo SC uptake of a model compound
D B Harper
The International journal of biochemistry, 17(6), 677-683 (1985-01-01)
The purification and properties of an enzyme from Nocardia sp. which catalyses the conversion of p-hydroxybenzonitrile to p-hydroxybenzoic acid and ammonia without intermediate formation of the amide is described. The enzyme displayed a broad pH optimum between 7.0 and 9.5
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