ChemicalBook--->CAS DataBase List--->14543-43-2

14543-43-2

14543-43-2 Structure

14543-43-2 Structure
IdentificationBack Directory
[Name]

2-AMINO-4-CYANO-PHENOL
[CAS]

14543-43-2
[Synonyms]

2-AMINO-4-CYANO-PHENOL
2-Amino-5-cyano-phenol
5-Cyano-2-hydroxy-aniline
3-Amino-4-hydroxybenzonitrile
Benzonitrile, 3-amino-4-hydroxy-
3-amino-4-hydroxybenzonitrile(SALTDATA: FREE)
5-Cyano-2-hydroxyaniline, 2-Amino-4-cyanophenol
5-Cyano-2-hydroxyaniline, 2-Amino-5-cyanophenol
[Molecular Formula]

C7H6N2O
[MDL Number]

MFCD00234273
[MOL File]

14543-43-2.mol
[Molecular Weight]

134.14
Chemical PropertiesBack Directory
[Melting point ]

151-153℃
[Boiling point ]

345.1±32.0 °C(Predicted)
[density ]

1.33±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

7.63±0.18(Predicted)
[color ]

Brown
[Sensitive ]

Air Sensitive
[Stability:]

Air Sensitive, Light Sensitive
[InChI]

InChI=1S/C7H6N2O/c8-4-5-1-2-7(10)6(9)3-5/h1-3,10H,9H2
[InChIKey]

ZEWCASRNRWXXSO-UHFFFAOYSA-N
[SMILES]

C(#N)C1=CC=C(O)C(N)=C1
[CAS DataBase Reference]

14543-43-2
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Warning
[Hazard statements ]

H301-H311-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P301+P310a-P305+P351+P338-P405-P501a
[Risk Statements ]

20/21/22-36/37/38
[Safety Statements ]

26-36/37/39
[RIDADR ]

3439
[HazardClass ]

6.1
[PackingGroup ]

Ⅲ
[HS Code ]

2926907090
Spectrum DetailBack Directory
[Spectrum Detail]

2-AMINO-4-CYANO-PHENOL(14543-43-2)1HNMR
2-AMINO-4-CYANO-PHENOL(14543-43-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Hydroxy-3-nitrobenzonitrile

3272-08-0

2-AMINO-4-CYANO-PHENOL

14543-43-2

Steps for the synthesis of 3-amino-4-hydroxybenzonitrile: 4-hydroxy-3-nitrobenzonitrile (10 g, 61 mmol) was dissolved in methanol (200 mL) at room temperature and 5% Pd/activated carbon catalyst (0.5 g) was added. Hydrogen was continuously passed into the reaction system via a hydrogen balloon for 24 hours. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated to afford the target product 3-amino-4-hydroxybenzonitrile (8.2 g, 100% yield).

[References]

[1] Patent: US6207697, 2001, B1
[2] Patent: US5886044, 1999, A
[3] Patent: US5780483, 1998, A
[4] Patent: US6262113, 2001, B1
[5] Bioorganic and Medicinal Chemistry Letters, 2001, vol. 11, # 12, p. 1545 - 1548
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