715670
2-(溴乙酰基)苯并呋喃
97%
别名:
1-(1-Benzofuran-2-yl)-2-bromoethan-1-one, 1-(1-Benzofuran-2-yl)-2-bromoethanone, 1-(2-Benzofuryl)-2-bromo-1-ethanone, 1-(Benzo[b]furan-2-yl)-2-bromoethan-1-one, 1-(Benzofuran-2-yl)-2-bromoethanone, 1-Benzo[b]furan-2-yl-2-bromoethanone, 2-(2-Bromoacetyl)benzofuran, 2-(Bromoacetyl)benzo[b]furan, 2-Benzofuranyl bromomethyl ketone, 2-Benzofuryl bromomethyl ketone
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关于此项目
经验公式（希尔记法）:
C10H7BrO2
化学文摘社编号:
分子量:
239.07
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
Quality Segment
assay
97%
form
solid
mp
86-90 °C
functional group
bromo, ketone
SMILES string
BrCC(=O)c1cc2ccccc2o1
InChI
1S/C10H7BrO2/c11-6-8(12)10-5-7-3-1-2-4-9(7)13-10/h1-5H,6H2
InChI key
NVRNCBWTEDOAQA-UHFFFAOYSA-N
Application
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
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable