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质量水平
反应适用性
reaction type: Grignard Reaction
浓度
1.0 M in THF
密度
1.021 g/mL at 25 °C
SMILES字符串
Fc1ccc([Mg]Br)cc1
InChI
1S/C6H4F.BrH.Mg/c7-6-4-2-1-3-5-6;;/h2-5H;1H;/q;;+1/p-1
InChI key
QYBFFRXNNFXREA-UHFFFAOYSA-M
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应用
4-氟苯基溴化镁溶液(格氏试剂)可用作合成以下化合物的试剂:
- 帕罗西汀合成中的关键中间体。
- 通过与硫醇的交叉偶联反应生成芳基硫化物。
- 作为雄激素受体拮抗剂的4-芳基甲基-1-苯基吡唑和4-芳氧基-1-苯基吡唑衍生物。
- 用于制备阿瑞吡坦的Grignard 中间体。
警示用语:
Danger
危险分类
Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3
靶器官
Respiratory system
补充剂危害
WGK
WGK 3
闪点(°F)
closed cup
闪点(°C)
closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
Design, synthesis, and biological evaluation of 4-arylmethyl-1-phenylpyrazole and 4-aryloxy-1-phenylpyrazole derivatives as novel androgen receptor antagonists
Bioorganic & Medicinal Chemistry, 20(7), 2338-2352 (2012)
Enantioselective synthesis of 3-substituted-4-aryl piperidines useful for the preparation of paroxetine
Tetrahedron Letters, 44(28), 5355-5358 (2003)
Understanding the origin of unusual stepwise hydrogenation kinetics in the synthesis of the 3-(4-fluorophenyl) morpholine moiety of NK1 receptor antagonist aprepitant
Organic Process Research & Development, 10(1), 109-117 (2006)
Journal of medicinal chemistry, 34(5), 1728-1731 (1991-05-01)
The synthesis and pharmacological characterization of a series of N-substituted 3-(4-fluorophenyl)tropane derivatives is reported. The compounds displayed binding characteristics that paralleled those of cocaine, and several had substantially higher affinity at cocaine recognition sites. Conjugate addition of 4-fluorophenyl magnesium bromide
The Journal of organic chemistry, 77(22), 10369-10374 (2012-10-17)
A convenient one-pot approach for the synthesis of aryl sulfides through the coupling of thiols with Grignard reagents in the presence of N-chlorosuccinimide is described. The sulfenylchlorides were formed when thiols were treated with N-chlorosuccinimide, and the resulting sulfenylchlorides were
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