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ChemicalBook--->CAS DataBase List--->2843-27-8

2843-27-8

2843-27-8 Structure

2843-27-8 Structure
IdentificationBack Directory
[CAS]

2843-27-8
[Molecular Formula]

C7H7NO2
[Molecular Weight]

137.14
Chemical PropertiesBack Directory
[Melting point ]

182-183 °C
[Boiling point ]

338.4±25.0 °C(Predicted)
[density ]

1.310±0.06 g/cm3(Predicted)
[storage temp. ]

-20°C
[solubility ]

DMF: 1 mg/mL,DMSO: 1 mg/mL,PBS (pH 7.2): 0.16 mg/mL
[form ]

A solid
[pka]

9.19±0.35(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H315-H319
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
Hazard InformationBack Directory
[Uses]

N-Formyl-2-aminophenol (N-(2-hydroxyphenyl)methanamide) is a bacterial secondary metabolite that has been found in P. chrysogenum and has antioxidant activity[1].
[Biological Activity]

N-formyl-2-Aminophenol is a bacterial secondary metabolite that has been found in P. chrysogenum and has antioxidant activity.1,2 It scavenges DPPH radicals in a cell-free assay with an IC50 value of 3.23 μg/ml.2 N-formyl-2-Aminophenol has also been used in the synthesis of compounds with antibacterial and antifungal activities.3
[References]

1.Frisvad, J.C., Smedsgaard, J., Larsen, T.O., et al.Mycotoxins, drugs and other extrolites produced by species in Penicillium subgenus PenicilliumStud. Mycol.49201-241(2004) 2.Deepali, A., Akansha, A., Anamika, B., et al.Hydroxylamine hydrochloride as an effective catalyst for form amide derivative synthesis and their DPPH scavenging activityRes. J. Chem. Sci.4(10)54-57(2014) 3.Gupta, S., Verma, P., and Singh, V.Synthesis and antimicrobial study of 2-amino-imidazole derivativesIndian J. Chem. 57B679-686(2018)
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