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Chemical Structure| 355423-58-4 Chemical Structure| 355423-58-4
Chemical Structure| 355423-58-4

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6-Bromo-7-fluoro-2H-benzo[b][1,4]oxazin-3(4H)-one

CAS No.: 355423-58-4

4.5 *For Research Use Only !

Cat. No.: A402848 Purity: 98%

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Product Details of [ 355423-58-4 ]

CAS No. :355423-58-4
Formula : C8H5BrFNO2
M.W : 246.03
SMILES Code : O=C1COC2=CC(F)=C(Br)C=C2N1
MDL No. :MFCD20441932
Boiling Point : No data available
InChI Key :AVHJMSMGASUDIT-UHFFFAOYSA-N
Pubchem ID :23574320

Safety of [ 355423-58-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H315-H319-H332-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis [ 355423-58-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 355423-58-4 ]

[ 355423-58-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 103361-99-5 ]
  • [ 355423-58-4 ]
YieldReaction ConditionsOperation in experiment
44% With N-Bromosuccinimide; In acetonitrile; at 20℃; for 5h; INTERMEDIATE 76-Bromo-7-fluoro-4H-benzori.4]oxazin-3-oneTo a solution of Intermediate 6 (4.1 g, 25.0 mmol) in MeCN (120 mL) was added NBS (5.41 g, 30 mmol). The reaction mixture was stirred for 4 h at r.t. before addition of further NBS (0.45 g, 2.5 mmol) and MeCN (30 mL) and stirring for a further 1 h. It was then concentrated in vacuo. The resulting residue was slurried in water (10O mL). The solid material was filtered off, washed with water and dried in vacuo to give the title compound (2.7 g, 44%) as an off-white solid. deltaeta (DMSO-d6) 10.81 (IH, s), 7.12 (IH, d, J 9.4 Hz), 7.09 (IH, d, J 7.0 Hz), 4.63 (2H, s).
 

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• Acyl Group Substitution • Alkyl Halide Occurrence • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Chan-Lam Coupling Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Fischer Indole Synthesis • General Reactivity • Grignard Reaction • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Kinetics of Alkyl Halides • Kumada Cross-Coupling Reaction • Lawesson's Reagent • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Peterson Olefination • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Amines • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Dihalides • Reformatsky Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Carbodiimides and Related Reagents • Specialized Acylation Reagents-Ketenes • Stille Coupling • Stobbe Condensation • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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