ChemicalBook--->CAS DataBase List--->18495-14-2

18495-14-2

18495-14-2 Structure

18495-14-2 Structure
IdentificationBack Directory
[Name]

2-HYDROXY-4-METHYL-BENZONITRILE
[CAS]

18495-14-2
[Synonyms]

2-HYDROXY-4-METHYL-BENZONITRILE
2-Hydroxy-4-methyk-benzonitrile
Benzonitrile, 2-hydroxy-4-Methyl-
[Molecular Formula]

C8H7NO
[MDL Number]

MFCD02261941
[MOL File]

18495-14-2.mol
[Molecular Weight]

133.15
Chemical PropertiesBack Directory
[Melting point ]

87 °C
[Boiling point ]

286.0±28.0 °C(Predicted)
[density ]

1.17±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

7.28±0.10(Predicted)
[Appearance]

Light brown to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2926907090
Spectrum DetailBack Directory
[Spectrum Detail]

2-HYDROXY-4-METHYL-BENZONITRILE(18495-14-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Benzaldehyde, 2-hydroxy-4-methyl-, oxime

84159-60-4

2-HYDROXY-4-METHYL-BENZONITRILE

18495-14-2

2-Hydroxy-4-methylbenzaldehyde oxime (23 g) was added to 190 mL of acetic anhydride. The reaction mixture was heated to reflux for 2 hours. After completion of the reaction, the mixture was concentrated and the residue was poured into ice water. The aqueous phase was extracted with ethyl acetate and the organic phase was combined. The organic phase was dried over anhydrous sodium sulfate, concentrated, and separated and purified by silica gel column chromatography to finally obtain 2-hydroxy-4-methylbenzonitrile (16 g).

[References]

[1] Journal of the Chemical Society, 1949, p. 885,889
[2] Patent: CN108117510, 2018, A. Location in patent: Paragraph 0020; 0023; 0024
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