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Chemical Structure| 1065101-52-1 Chemical Structure| 1065101-52-1

Structure of 1065101-52-1

Chemical Structure| 1065101-52-1

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Product Details of [ 1065101-52-1 ]

CAS No. :1065101-52-1
Formula : C6H3F3IN
M.W : 272.99
SMILES Code : NC1=C(F)C=C(F)C(F)=C1I
MDL No. :MFCD11054254
InChI Key :NLBADBUEJHRKAI-UHFFFAOYSA-N
Pubchem ID :79022208

Safety of [ 1065101-52-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362

Application In Synthesis of [ 1065101-52-1 ]

* 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 [ 1065101-52-1 ]

[ 1065101-52-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 367-34-0 ]
  • [ 1065101-52-1 ]
  • C6H3F3IN [ No CAS ]
  • C6H2F3I2N [ No CAS ]
YieldReaction ConditionsOperation in experiment
43%; 8%; 32% With iodine; silver sulfate; In ethanol;Reflux; General procedure: Method II. A solution of 2,3,5-trifluoro-4-(trifluoromethyl)aniline 1a (0.34 g, 1.57 mmol) in EtOH (3 mL) was added during 15 min to a stirred mixture of I2 (0.51 g, 2.0 mmol), Ag2SO4 (0.62 g, 2.0 mmol) and EtOH (10 mL). The mixture was boiled for 4 h, filtered, solvent was evaporated. The residue was dissolved in CHCl3 (40 mL), the solution was washed with sat. aq. solutions of Na2S2O3 (2 .x. 30 mL) and NaCl (30 mL), then with H2O (30 mL), dried (MgSO4), and purified by flash chromatography on Al2O3 to afford 2a (0.49 g, 93percent) as an oil.
  • 2
  • [ 367-34-0 ]
  • [ 1065101-52-1 ]
YieldReaction ConditionsOperation in experiment
97% With iodine; iodic acid; In 1,4-dioxane; water; for 3h;Reflux; General procedure: To a stirred solution of aniline 1a (0.52 g, 2.4 mmol) in dioxane (18 mL) at 70 °C were added 0.31 (1.2 mmol) fine-ground iodine and a solution of iodic acid (0.43 g, 2.4 mmol) in H2O (3 mL). The reaction mixture was refluxed for 4 h, cooled to r.t., poored into H2O (50 mL) and extracted with CHCl3 (3 .x. 30 mL). The extract was washed with sat. Na2S2O3 (2 .x. 30 mL) and NaCl (30 mL) solutions, then with H2O (30 mL), dried (MgSO4), and purified by flash chromatography on Al2O3 to afford 2a (0.79 g, 97percent) as an oil.
With iodine; iodic acid; In 1,4-dioxane; water; for 5h;Reflux; General procedure: To a stirred solution of aniline 1 (8 mmol) in 1,4-dioxane (60 mL) were added a solution of HIO3 (2.8 g, 16 mmol) in H2O (20 mL) and then finely ground I2 (2.0 g, 8 mmol). The reaction mixture was refluxed for 5 h, cooled to r.t., poured into H2O (50 mL), and extracted with CH2Cl2 (3 × 70 mL). The combined organic layers were washed with sat. aq Na2S2O3 (2 × 50 mL), H2O (2 × 70 mL), dried (MgSO4), and purified by flash chromatography on Al2O3 using CH2Cl2 as the eluent.
 

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• Alkyl Halide Occurrence • Arndt-Eistert Homologation • 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 • Hunsdiecker-Borodin Reaction • Hydride Reductions • Kinetics of Alkyl Halides • 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 • Preparation of Carboxylic Acids • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Carboxylic Acids • Reactions of Dihalides • Reformatsky Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Ketenes • Specialized Acylation Reagents-Vilsmeier Reagent • Stobbe Condensation • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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