All Photos(2)
Synonym(s):
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
Empirical Formula (Hill Notation):
C10H7BrO2
CAS Number:
Molecular Weight:
239.07
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
97%
form
solid
mp
86-90 °C
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
Related Categories
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
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A Veeraiah
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 147, 212-224 (2015-04-05)
The vibrational and electronic properties of 2-(bromoacetyl)benzo(b)furan have been studied in the ground state using experimental techniques (FT-IR, FT-Raman and UV) and density functional theory (DFT) employing B3LYP exchange correlation with the 6-31G(d,p) basis set. The theoretically calculated optimized parameters
Justin D Smith et al.
Nature communications, 10(1), 1837-1837 (2019-04-25)
Photocatalytic polymers offer an alternative to prevailing organometallics and nanomaterials, and they may benefit from polymer-mediated catalytic and material enhancements. MPC-1, a polymer photoredox catalyst reported herein, exhibits enhanced catalytic activity arising from charge transfer states (CTSs) between its two
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