561037
3,4-Difluorophenylmagnesium bromide solution
0.5 M in THF
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About This Item
Fórmula lineal:
F2C6H3MgBr
Número de CAS:
Peso molecular:
217.29
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
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reaction suitability
reaction type: Grignard Reaction
Quality Level
concentration
0.5 M in THF
bp
65 °C
density
0.965 g/mL at 25 °C
storage temp.
2-8°C
SMILES string
Fc1ccc([Mg]Br)cc1F
InChI
1S/C6H3F2.BrH.Mg/c7-5-3-1-2-4-6(5)8;;/h1,3-4H;1H;/q;;+1/p-1
InChI key
WZHAVYGMKGPNFN-UHFFFAOYSA-M
Categorías relacionadas
Application
3,4-Difluorophenylmagnesium bromide can be used:
- To prepare 3,4-difluorophenylboronic acid, a key building block employed in the synthesis of norepinephrine transporter selective molecules.
- In the synthesis of trimethoxybenzophenone derived tubulin polymerization inhibitors.
- In one of the key synthetic steps for the preparation of diarylketoxime derivatives as potent MCH-1R antagonists.
- In the synthesis of biologically important hydroxybupropion analogs useful in smoking cessation.
Legal Information
Product of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
target_organs
Respiratory system
supp_hazards
Storage Class
3 - Flammable liquids
wgk_germany
WGK 3
flash_point_f
1.0 °F - closed cup
flash_point_c
-17.2 °C - closed cup
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Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
Synthesis and characterization of in vitro and in vivo profiles of hydroxybupropion analogues: aids to smoking cessation
Lukas RJ, et al.
Journal of Medicinal Chemistry, 53(12), 4731-4748 (2010)
Synthesis and monoamine transporter binding properties of 3α-(substituted phenyl) nortropane-2β-carboxylic acid methyl esters. Norepinephrine transporter selective compounds
Carroll FI, et al.
Journal of medicinal chemistry, 48(11), 3852-3857 (2005)
Discovery of novel diarylketoxime derivatives as selective and orally active melanin-concentrating hormone 1 receptor antagonists
Suzuki T, et al.
Bioorganic & medicinal chemistry letters, 19(18), 5339-5345 (2009)
2?Amino?3, 4, 5?Trimethoxybenzophenones as Potent Tubulin Polymerization Inhibitors.
Chuang H Y, et al.
ChemMedChem, 6(3), 450-456 (2011)
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