ChemicalBook--->CAS DataBase List--->13589-72-5

13589-72-5

13589-72-5 Structure

13589-72-5 Structure
IdentificationMore
[Name]

5-CHLORO-2-HYDROXYBENZONITRILE
[CAS]

13589-72-5
[Synonyms]

5-CHLORO-2-HYDROXYBENZONITRILE
AKOS B029245
5-Chloro-2-hydroxybenzonitrile, tech
4-Chloro-2-cyanophenol
[Molecular Formula]

C7H4ClNO
[MDL Number]

MFCD00219003
[Molecular Weight]

153.57
[MOL File]

13589-72-5.mol
Chemical PropertiesBack Directory
[Melting point ]

152-154°C
[Boiling point ]

269.4±25.0 °C(Predicted)
[density ]

1.41±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

6.72±0.18(Predicted)
[Appearance]

Light brown to off-white Solid
[CAS DataBase Reference]

13589-72-5(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

H301+H311+H331-H315-H319
[Precautionary statements ]

P501-P261-P270-P271-P264-P280-P337+P313-P305+P351+P338-P361+P364-P332+P313-P301+P310+P330-P302+P352+P312-P304+P340+P311-P403+P233-P405
[Hazard Codes ]

Xi
[Risk Statements ]

R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[RIDADR ]

3276
[HS Code ]

2926907090
Spectrum DetailBack Directory
[Spectrum Detail]

5-CHLORO-2-HYDROXYBENZONITRILE(13589-72-5)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

5-chloro-2-hydroxybenzonitrile(13589-72-5)
Hazard InformationBack Directory
[Synthesis]

5-Chlorosalicylaldehyde

635-93-8

5-CHLORO-2-HYDROXYBENZONITRILE

13589-72-5

The general procedure for the synthesis of 5-chloro-2-hydroxybenzonitrile from 5-chlorosalicylaldehyde is as follows: 1. 5-Chloro-2-hydroxybenzaldehyde (300 g, 1.92 mol) was suspended in water (4.5 L) with hydroxylamine-O-sulfonic acid (260 g, 2.30 mol) at room temperature. 2. The reaction mixture was stirred at 60 °C for 7 hours. 3. Upon completion of the reaction, water (3 L) was added to the mixture, which was subsequently chilled with ice. 4. The precipitated crystals were collected by filtration and washed with 1.5 L of water. 5. The resulting crystals were re-suspended in 1.5 L of water, filtered and washed with water. 6. 6. Finally, the crystals were tray dried at 50 °C for 22 h to give 272 g of 5-chloro-2-hydroxybenzonitrile (white crystals, yield: 93%). The structure of the product was confirmed by 1H-NMR (CDCl3): δ 6.94 (1H, d, J = 8.8 Hz), 7.42 (1H, dd, J = 8.8,2.9 Hz), 7.47 (1H, d, J = 2.9 Hz).

[References]

[1] Patent: WO2006/115130, 2006, A1. Location in patent: Page/Page column 53-54
[2] Patent: US2007/117866, 2007, A1
[3] Gazzetta Chimica Italiana, 1959, vol. 89, p. 1009,1013
[4] Journal of Molecular Recognition, 2012, vol. 25, # 6, p. 352 - 360
[5] Journal of Organic Chemistry, 2015, vol. 80, # 2, p. 1229 - 1234
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