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Chemical Structure| 1197377-31-3 Chemical Structure| 1197377-31-3

Structure of 1197377-31-3

Chemical Structure| 1197377-31-3

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Product Details of [ 1197377-31-3 ]

CAS No. :1197377-31-3
Formula : C16H15ClN2O3
M.W : 318.75
SMILES Code : O=C(CC1)N(C(O)C(Cl)CC2=CC=C3N=CC=CC3=C2)C1=O
MDL No. :MFCD30489249
InChI Key :FUPWOFWDARMISK-UHFFFAOYSA-N
Pubchem ID :44512897

Safety of [ 1197377-31-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 1197377-31-3 ]

* 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 [ 1197377-31-3 ]

[ 1197377-31-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 709652-82-4 ]
  • [ 1197377-31-3 ]
  • 6-bromo-3-(quinolin-6-ylmethyl)imidazo[1,2-a]pyridine-8-carbonitrile [ No CAS ]
  • 2
  • [ 709652-82-4 ]
  • [ 1197377-31-3 ]
  • 6-(1-methyl-1H-pyrazol-4-yl)-3-(quinolin-6-ylmethyl)imidazo[1,2-a]pyridine-8-carbonitrile [ No CAS ]
 

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Technical Information

• Acyl Group Substitution • Alkyl Halide Occurrence • Appel Reaction • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chan-Lam Coupling Reaction • Chugaev Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Corey-Kim Oxidation • Dess-Martin Oxidation • Fischer Indole Synthesis • General Reactivity • Grignard Reaction • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Jones Oxidation • Kinetics of Alkyl Halides • Kumada Cross-Coupling Reaction • Lawesson's Reagent • Leuckart-Wallach Reaction • Martin's Sulfurane Dehydrating Reagent • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mitsunobu Reaction • Moffatt Oxidation • Oxidation of Alcohols by DMSO • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Peterson Olefination • 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 Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions with Organometallic Reagents • Reformatsky Reaction • Ritter Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Sharpless Olefin Synthesis • Specialized Acylation Reagents-Carbodiimides and Related Reagents • Specialized Acylation Reagents-Ketenes • Stille Coupling • Stobbe Condensation • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Swern Oxidation • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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