539392
2-溴-4′-氰基苯乙酮
96%
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关于此项目
线性分子式:
BrCH2COC6H4CN
化学文摘社编号:
分子量:
224.05
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
2-溴-4′-氰基苯乙酮, 96%
assay
96%
InChI
1S/C9H6BrNO/c10-5-9(12)8-3-1-7(6-11)2-4-8/h1-4H,5H2
SMILES string
BrCC(=O)c1ccc(cc1)C#N
InChI key
LJANCPRIUMHGJE-UHFFFAOYSA-N
mp
92-96 °C (lit.)
functional group
bromo
ketone
nitrile
Quality Level
Application
2-Bromo-4′-cyanoacetophenone may be used to synthesize:
- 3-acylindolizines
- (2R,3R)-3-[4-(4-cyanophenyl)thiazol-2-yl]-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-2-butanol
- 1-[2-(4-cyanophenyl)-2-oxoethyl]-1,10-phenanthrolinium bromide
General description
2-Bromo-4′-cyanoacetophenone can be synthesized from ethylbenzene via aerobic photooxidation using aqueous HBr.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Application of DMF?methyl sulfate adduct in the regioselective synthesis of 3-acylated indolizines.
Przewloka T, et al.
Tetrahedron Letters, 48(33), 5739-5742 (2007)
New 1, 10-phenanthroline derivatives with potential antitumoral activity.
Dumitrascu F, et al.
Rev. Roum. Chim., 53(3), 183-187 (2008)
Synthesis and antifungal activity of novel thiazole-containing triazole antifungals. II. Optically active ER-30346 and its derivatives.
Tsuruoka, Akihiko, et al.
Chemical & Pharmaceutical Bulletin, 46(4), 623-630 (1998)
Norihiro Tada et al.
Organic & biomolecular chemistry, 8(20), 4701-4704 (2010-08-27)
The direct synthesis of α-bromoketones from alkylarenes by aerobic photooxidation with hydrobromic acid is reported. The key success for this direct oxidative reaction is due to control of bromination with acetic acid and ethanol, which are generated in situ by
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