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Chemical Structure| 106578-01-2 Chemical Structure| 106578-01-2

Structure of 106578-01-2

Chemical Structure| 106578-01-2

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Product Details of [ 106578-01-2 ]

CAS No. :106578-01-2
Formula : C11H6Br2O3
M.W : 345.97
SMILES Code : O=C1C(C(CBr)=O)=CC2=C(O1)C=CC(Br)=C2
MDL No. :MFCD00634768

Safety of [ 106578-01-2 ]

Application In Synthesis of [ 106578-01-2 ]

* 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 [ 106578-01-2 ]

[ 106578-01-2 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 36822-11-4 ]
  • [ 106578-01-2 ]
  • [ 1233880-65-3 ]
  • 2
  • [ 30748-47-1 ]
  • [ 106578-01-2 ]
  • [ 2231-57-4 ]
  • (E)-3-(2-(2-(1-(2-amino-4-methylthiazol-5-yl)ethylidene)hydrazinyl)-6H-1,3,4-thiadiazin-5-yl)-6-bromo-2H-chromen-2-one [ No CAS ]
  • 3
  • [ 30748-47-1 ]
  • [ 106578-01-2 ]
  • [ 79-19-6 ]
  • (E)-3-(2-(2-(1-(2-amino-4-methylthiazol-5-yl)ethylidene)hydrazinyl)thiazol-4-yl)-6-bromo-2H-chromen-2-one [ No CAS ]
 

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Technical Information

• Acyl Group Substitution • Alkyl Halide Occurrence • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bouveault-Blanc Reduction • Bucherer-Bergs Reaction • Catalytic Hydrogenation • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Ester Cleavage • 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 • Reactions with Organometallic Reagents • 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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