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Chemical Structure| 1234014-65-3 Chemical Structure| 1234014-65-3

Structure of 1234014-65-3

Chemical Structure| 1234014-65-3

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Product Details of [ 1234014-65-3 ]

CAS No. :1234014-65-3
Formula : C6H4Br2N2O
M.W : 279.92
SMILES Code : O=CNC1=C(Br)C=C(Br)N=C1
MDL No. :MFCD28400914

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Application In Synthesis of [ 1234014-65-3 ]

* 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 [ 1234014-65-3 ]

[ 1234014-65-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 50786-37-3 ]
  • [ 64-18-6 ]
  • [ 1234014-65-3 ]
YieldReaction ConditionsOperation in experiment
With acetic anhydride; at 0 - 20℃; To a stirred solution of compound 208.1 (350 mg) in formic acid (2.2 ml) was added acetic anhydride (1.2 ml) at 0 C and stirred at room temperature for 5 hr. After completion of the starting material (by TLC), the reaction mixture was concentrated under reduced pressure to afford compound 208.2 (250 mg, 64%) of a white solid which was used immediately in the next step without further purification. H-NMR (CDCl3, 500 MHz) delta 9.37 (s, 1H), 8.52 (s, 1H), 7.73 (s, 1H), 7.25 (bs, 1H).
 

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Technical Information

• Alkyl Halide Occurrence • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chan-Lam Coupling Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Fischer Indole Synthesis • General Reactivity • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Julia-Kocienski Olefination • Kinetics of Alkyl Halides • Knoevenagel Condensation • Kumada Cross-Coupling Reaction • Leuckart-Wallach Reaction • Mannich Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mukaiyama Aldol Reaction • Nozaki-Hiyama-Kishi Reaction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • 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 • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Vilsmeier Reagent • Stetter Reaction • 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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