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Chemical Structure| 60484-29-9 Chemical Structure| 60484-29-9

Structure of 60484-29-9

Chemical Structure| 60484-29-9

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Product Details of [ 60484-29-9 ]

CAS No. :60484-29-9
Formula : C11H10N2O2
M.W : 202.21
SMILES Code : O=CC1=C(O)N(C2=CC=CC=C2)N=C1C
MDL No. :MFCD00448479

Safety of [ 60484-29-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 60484-29-9 ]

* 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 [ 60484-29-9 ]

[ 60484-29-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 773-76-2 ]
  • [ 5970-45-6 ]
  • [ 60484-29-9 ]
  • ((4-formyl-3-methyl-1-phenyl-1H-pyrazol-5-yl)oxy)(5,7-dichloroquinolin-8-yloxy)zinc(II) [ No CAS ]
YieldReaction ConditionsOperation in experiment
68% In ethanol; at 70℃; General procedure: The complexes were synthesized byDBHQ(0.303 g, 1mmol) or DCHQ (0.214 g, 1 mmol) and secondary ligand (L) (0.202 g, 1 mmol) in absolute ethanol at 70 C followed by dropwise addition of zinc acetate dihydrate (0.219 g, 1 mmol) in 10 ml of same solvent at 70 C with continuous stirring and pale yellow colored precipitates were obtained. Wash with deionized water to remove excess metal ions and then wash with absolute ethanol followed by diethyl ether and dried it.
 

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Technical Information

• Appel Reaction • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chugaev Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Corey-Kim Oxidation • Dess-Martin Oxidation • Fischer Indole Synthesis • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Jones Oxidation • Julia-Kocienski Olefination • Knoevenagel Condensation • Leuckart-Wallach Reaction • Martin's Sulfurane Dehydrating Reagent • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mitsunobu Reaction • Moffatt Oxidation • Mukaiyama Aldol Reaction • Nozaki-Hiyama-Kishi Reaction • Oxidation of Alcohols by DMSO • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Alcohols • Preparation of Aldehydes and Ketones • Preparation of Amines • Prins Reaction • Reactions of Alcohols • Reactions of Aldehydes and Ketones • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions with Organometallic Reagents • Reformatsky Reaction • Ritter Reaction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Sharpless Olefin Synthesis • Stetter Reaction • Stobbe Condensation • Swern Oxidation • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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