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[ CAS No. 3984-34-7 ] {[proInfo.proName]}

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Chemical Structure| 3984-34-7
Chemical Structure| 3984-34-7
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Product Details of [ 3984-34-7 ]

CAS No. :3984-34-7 MDL No. :MFCD00002794
Formula : C10H9ClO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :AHVASTJJVAYFPY-UHFFFAOYSA-N
M.W : 212.63 Pubchem ID :77604
Synonyms :

Safety of [ 3984-34-7 ]

Signal Word:Warning Class:
Precautionary Statements:P305+P351+P338 UN#:
Hazard Statements:H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 3984-34-7 ]

* 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 [ 3984-34-7 ]

[ 3984-34-7 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 13754-19-3 ]
  • [ 3984-34-7 ]
  • 8a-(4'-Chlorophenyl)-7,8,8a,9-tetrahydro-6H-pyrrolo<2,1-f>purin-6-one [ No CAS ]
  • 2
  • [ 3984-34-7 ]
  • [ 2166-13-4 ]
YieldReaction ConditionsOperation in experiment
With hydrazine; In ethanol; 6-(4-Chlorophenyl)pyridazin-3-one Hydrazine (8.9 mL, 0.28 mol) was added to a suspension of 3-(4-chlorobenzoyl)propionic acid (30.0 g, 0.14 mol) in EtOH. The resulting mixture was heated to reflux for 1 hour, stirred at room temperature overnight and chilled with an ice bath. The title compound precipitated out of this mixture (23.85 g, 81%) as a yellow solid: mp 175-176 C. The following pyridazin-3-ones listed in Table 1 were prepared essentially by the above procedure, using the appropriate starting materials.
  • 3
  • [ 3984-34-7 ]
  • [ 19008-43-6 ]
  • [ 1191053-03-8 ]
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Technical Information

? Alkyl Halide Occurrence ? Arndt-Eistert Homologation ? Baeyer-Villiger Oxidation ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bucherer-Bergs Reaction ? Clemmensen Reduction ? Corey-Bakshi-Shibata (CBS) Reduction ? Corey-Chaykovsky Reaction ? Fischer Indole Synthesis ? Friedel-Crafts Reaction ? General Reactivity ? Grignard Reaction ? Henry Nitroaldol Reaction ? Hiyama Cross-Coupling Reaction ? Horner-Wadsworth-Emmons Reaction ? Hunsdiecker-Borodin Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? 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 Alkylbenzene ? Preparation of Amines ? Preparation of Carboxylic Acids ? Prins Reaction ? Reactions of Aldehydes and Ketones ? Reactions of Alkyl Halides with Reducing Metals ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reactions of Carboxylic Acids ? Reformatsky Reaction ? Robinson Annulation ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Specialized Acylation Reagents-Ketenes ? Stille Coupling ? Stobbe Condensation ? Substitution and Elimination Reactions of Alkyl Halides ? Suzuki Coupling ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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