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Chemical Structure| 110837-53-1 Chemical Structure| 110837-53-1

Structure of 110837-53-1

Chemical Structure| 110837-53-1

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Product Details of [ 110837-53-1 ]

CAS No. :110837-53-1
Formula : C9H8ClNO4
M.W : 229.62
SMILES Code : O=CC1=CC([N+]([O-])=O)=CC=C1OCCCl
MDL No. :MFCD21606627

Safety of [ 110837-53-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 110837-53-1 ]

* 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 [ 110837-53-1 ]

[ 110837-53-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 110837-53-1 ]
  • [ 3321-92-4 ]
  • C17H12Cl3NO5 [ No CAS ]
YieldReaction ConditionsOperation in experiment
89% With potassium hydroxide; In ethanol; at 20℃; for 48h; General procedure: A mixture of A & B (0.002 mol) and A' & B' (0.002 mol) was dissolved in 30 ml of ethanol and 10 ml of 40% KOH was added in 100 ml capacity conical flask. The reaction mixture was stirred at room temp for 48 hr. Then reaction mixture was poured over crushedice and content were acidified with conc. HCl. The yellow solid thus obtained was filtered and crystallizedfrom acetic acid to afford the pure compound 1 & 3. The same experimental procedure was followed to prepare other analogs of this series Table-1.
 

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• Alkyl Halide Occurrence • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs 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 • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mukaiyama Aldol Reaction • Nomenclature of Ethers • Nozaki-Hiyama-Kishi Reaction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Amines • Preparation of Ethers • 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 Ethers • Reformatsky Reaction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • 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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