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Chemical Structure| 105192-42-5 Chemical Structure| 105192-42-5

Structure of 105192-42-5

Chemical Structure| 105192-42-5

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Product Details of [ 105192-42-5 ]

CAS No. :105192-42-5
Formula : C12H9ClN2O
M.W : 232.67
SMILES Code : O=C(C1=CC=NC=C1)C2=CC(Cl)=CC=C2N
MDL No. :MFCD18409840

Safety of [ 105192-42-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 105192-42-5 ]

* 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 [ 105192-42-5 ]

[ 105192-42-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 872-85-5 ]
  • [ 65854-91-3 ]
  • [ 105192-42-5 ]
  • 2
  • [ 52482-36-7 ]
  • [ 65854-91-3 ]
  • [ 105192-42-5 ]
YieldReaction ConditionsOperation in experiment
65% 0111] Under a nitrogen atmosphere, <strong>[65854-91-3]N-(4-chlorophenyl)-2,2-dimethylpropionamide</strong> (6.5 g) and tetrahydrofuran (52 mL) were added, and the mixture was cooled to -30 C. 1.6M n-Butyllithium (n-BuLi) in hexane (48.1 mL) was added dropwise at -30 to -20 C., and the mixture was stirred for 2 hr and warmed to room temperature. A solution (20 mL) of morpholin-4-yl(pyridin-4-yl)methanone obtained in step 2 was added dropwise at 15-25 C., and tetrahydrofuran (5 mL) was added. After stirring at around room temperature for 4 hr, 15% aqueous ammonium chloride solution (33 mL) was added at 25 C. or below, and the organic layer was separated. To the organic layer was added 15% aqueous ammonium chloride solution (33 mL), and the mixture was partitioned. To the organic layer was added 10% brine (33 mL), and the mixture was partitioned. The organic layer was concentrated to about 20 mL under reduced pressure, and methanol (39 ml) was added. A solution of potassium hydroxide (8.62 g) in water (17 mL) was added at 20 C. or below. After stirring at 55-65 C. for 4 hr, the mixture was cooled to 5 C. or below, and the mixture was stirred for 1 hr. The crystals were collected by filtration, washed with a mixed solution of methanol (20 mL)/tetrahydrofuran (3.3 mL) cooled to 5 C. or below, and dried under reduced pressure to give the title compound as crystals. Standard yield: 65±10%
 

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Technical Information

• Alkyl Halide Occurrence • 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 • Clemmensen Reduction • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • 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 • Mannich 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 Benzene and Substituted Benzenes • Reformatsky Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Ketenes • Specialized Acylation Reagents-Vilsmeier Reagent • 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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