2-氟苯甲腈
2-氟苯甲腈结构式
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常用名 | 2-氟苯甲腈 | 英文名 | 2-Fluorobenzonitrile |
|---|---|---|---|---|
| CAS号 | 394-47-8 | 分子量 | 121.112 | |
| 密度 | 1.2±0.1 g/cm3 | 沸点 | 193.6±0.0 °C at 760 mmHg | |
| 分子式 | C7H4FN | 熔点 | 35 - 37ºC | |
| MSDS | 中文版 美版 | 闪点 | 73.9±0.0 °C | |
| 符号 |
GHS05, GHS07 |
信号词 | Danger |
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High-sensitivity elemental ionization for quantitative detection of halogenated compounds.
Analyst 140 , 8177-85, (2015) The rising importance of organohalogens in environmental, pharmaceutical, and biological applications has drawn attention to analysis of these compounds in recent years. Elemental mass spectrometry (MS) is particularly advantageous in this regard because of i... |
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Studies on the synthetic compatibility of aryloxime linkers in the solid-phase synthesis of 3-aminobenzisoxazoles.
J. Org. Chem. 65(10) , 2924-32, (2000) Further exploration of the scope of our solid-phase method for the synthesis of 3-aminobenzisoxazoles (using the Kaiser oxime resin 1) is described. The effects of base, leaving group, and solvent on the nucleophilic aromatic substitution based resin-loading ... |
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Aminoborohydrides. 12. Novel tandem S(N)Ar amination-reduction reactions of 2-halobenzonitriles with lithium N,N-dialkylaminoborohydrides.
J. Org. Chem. 66(6) , 1999-2004, (2001) A novel tandem amination-reduction reaction has been developed in which 2-(N,N-dialkylamino)benzylamines are generated from 2-halobenzonitriles and lithium N,N-dialkylaminoborohydride (LAB) reagents. These reactions are believed to occur through a tandem S(N)... |
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Synthesis of dixanthones and poly(dixanthone)s by cyclization of 2-aryloxybenzonitriles in trifluoromethanesulfonic acid.
Org. Lett. 3(15) , 2337-40, (2001) [reaction: see text] Condensation of 2-fluorobenzonitriles with phenoxides affords 2-aryloxybenzonitriles that cyclize cleanly in trifluoromethanesulfonic acid at room temperature to give xanthone-iminium triflates. The C=N bond in these compounds is remarkab... |
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Efficient synthesis of 5-(4'-methyl [1, 1'-biphenyl]-2-yl)-1H-tetrazole. Russell RK and Murray WV.
J. Org. Chem. 58(18) , 5023-24, (1993)
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