| Identification | More | [Name]
1-(1-BENZOFURAN-2-YL)-2-BROMOETHAN-1-ONE | [CAS]
23489-36-3 | [Synonyms]
1-(1-BENZOFURAN-2-YL)-2-BROMOETHAN-1-ONE
1-(1-BENZOFURAN-2-YL)-2-BROMOETHANONE
1-BENZOFURAN-2-YL-2-BROMO-ETHANONE
2-(2-BROMOACETYL)BENZOFURAN
AKOS BBS-00004078
2-(2-Bromoacetyl)benzo[b]furan
1-(1-Benzofuran-2-yl)-2-bromoethan-1-one, GC 90+%
1-(1-Benzofuran-2-yl)-2-bromoethan-1-one ,97% | [EINECS(EC#)]
200-258-5 | [Molecular Formula]
C10H7BrO2 | [MDL Number]
MFCD00176644 | [Molecular Weight]
239.07 | [MOL File]
23489-36-3.mol |
| Chemical Properties | Back Directory | [Appearance]
white to light yellow crystal powde | [Melting point ]
89 °C | [Boiling point ]
306.8±17.0 °C(Predicted) | [density ]
1.582±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [form ]
solid | [Detection Methods]
HPLC | [CAS DataBase Reference]
23489-36-3(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
C,Xi | [Risk Statements ]
R34:Causes burns. | [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 .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [RIDADR ]
3261 | [WGK Germany ]
2 | [Hazard Note ]
Corrosive | [HazardClass ]
IRRITANT | [HS Code ]
29329990 |
| Hazard Information | Back Directory | [Chemical Properties]
white to light yellow crystal powde | [Uses]
Reactant for:
- Eschenmoser coupling reaction
- Preparation of β-oxo sulfones as substrates for stereoselective Michael addition/cross-benzoin cascade reactions
- Preparation of thienylpyrazole-based thiazoles and pyrazolines as antimicrobial, antioxidant, anti-inflammatory, and analgesic agents
- Preparation of isatin-(benzofuryl-thiazolyl)-hydrazones by cyclocondensation with isatin-thiosemicarbazones under microwave irradiation as antimicrobial agents
- Synthesis of 2-naphthyl ethers as a protective agent against DNA damage induced by bleomycin-iron
- Asymmetric synthesis of β-dialkylamino alcohols by Ru-catalyzed transfer hydrogenation of α-dialkylamino ketones
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