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[ CAS No. 42951-39-3 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 42951-39-3
Chemical Structure| 42951-39-3
Chemical Structure| 42951-39-3
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Product Details of [ 42951-39-3 ]

CAS No. :42951-39-3 MDL No. :MFCD04972092
Formula : C17H25N Boiling Point : -
Linear Structure Formula :- InChI Key :MOVCYDNEZZZSLV-UHFFFAOYSA-N
M.W : 243.39 Pubchem ID :170708
Synonyms :

Safety of [ 42951-39-3 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 42951-39-3 ]

* 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 [ 42951-39-3 ]

[ 42951-39-3 ] Synthesis Path-Downstream   1~11

YieldReaction ConditionsOperation in experiment
... falling within the ambit of the formula 1-R8 -pyrrole and carbazole compounds falling within the ambit of the formula 9-R8 -carbazole which are useful in the practice of the processes of this invention for producing the aforesaid methanes and alkanes of Formulas I, XI and XVI. ... 2-Phenylindole, 1-Propyl-2-methylindole, 1-Benzyl-2-methylindole, 1-Butyl-2-methylindole, 1-Octyl-2-methylindole, 2-Ethyl-5-methylindole, 1-Benzyl-5-fluoroindole, 1-Methyl-6-nitroindole, ...
The following compounds are exemplary of indoles, pyrroles and carbazoles useful in the practice of this invention. ... 1-Benzyl-2-methylindole, 1-Butyl-2-methylindole, 1-Octyl-2-methylindole, 2-Ethyl-5-methylindole, ...
The following compounds are exemplary of indoles useful in the practice of this invention. ... 1,2-Dimethylindole, 1-Ethyl-2-methylindole, 1-Propyl-2-methylindole, 1-Butyl-2-methylindole, 1-Octyl-2-methylindole, 2-Ethylindole, 2-Ethyl-1-methylindole, 1-Isopropylindole, ...
The following compounds are exemplary of indoles, pyrroles and carbazoles useful in the practice of this invention. ... 2-Phenylindole, 1-Propyl-2-methylindole, 1-Benzyl-2-methylindole, 1-Butyl-2-methylindole, 1-Octyl-2-methylindole, 2-Ethyl-5-methylindole, 1-Benzyl-5-fluoroindole, 1-Methyl-6-nitroindole, ...
The following compounds are exemplary of indoles useful in the practice of this invention. ... 2-Phenylindole, 1-Propyl-2-methylindole, 1-Benzyl-2-methylindole, 1-Butyl-2-methylindole, 1-Octyl-2-methylindole, 2-Ethyl-5-methylindole, 1-Benzyl-5-fluoroindole, 1-Methyl-6-nitroindole, ...
2-Methylindol, n-Octylbromid, KOH/DMSO;

  • 2
  • [ 42951-39-3 ]
  • 1-dicyanomethylene-3-dimethylpropionyliminoisoindoline [ No CAS ]
  • 1-Dicyanomethylene-3-(2,2-dimethylpropionylamino)-3-(2-methyl-1-n-octylindol-3-yl)isoindoline [ No CAS ]
YieldReaction ConditionsOperation in experiment
With toluene-4-sulfonic acid In acetone; toluene 1 1-Dicyanomethylene-3-(2,2-dimethylpropionylamino)-3-(2-methyl- 1-n-octylindol-3-yl)isoindoline Example 1 1-Dicyanomethylene-3-(2,2-dimethylpropionylamino)-3-(2-methyl- 1-n-octylindol-3-yl)isoindoline 2.8 g of 1-dicyanomethylene-3-dimethylpropionyliminoisoindoline are stirred together with 2.43 g of 1-n-octyl-2-methylindole and 0.2 g of p-toluenesulfonic acid in 15 ml of toluene and 10 ml acetone at room temperature for 6 hours. This is followed by concentrating the solvent mixture, resulting in the formation of a precipitate. The precipitate is filtered off, washed with toluene and dried. 3 g of the compound of the formula STR17 are isolated as colourless crystals having a melting point of 178°-179° C. In thermography, this colour former develops a red-violet marking.
  • 3
  • [ 85-44-9 ]
  • [ 42951-39-3 ]
  • [ 60316-84-9 ]
YieldReaction ConditionsOperation in experiment
15.A EXAMPLE 15 A. Following a procedure similar to that described in Example 14A but employing 7.4 g. of phthalic anhydride and 16.0 g. of 1-n-octyl-2-methylindole there was obtained 6.9 g. of 2-(1-n-octyl-2-methyl-3-indolylcarbonyl)benzoic acid, m.p. 121°-123° C.
  • 4
  • [ 42951-39-3 ]
  • [ 21528-38-1 ]
  • [ 75-36-5 ]
  • 3-[2,2-bis(1-n-octyl-2-methylindol-3-yl)ethenyl]-3-(4-diethylaminophenyl)phthalide [ No CAS ]
YieldReaction ConditionsOperation in experiment
60.6% With calcium hydroxide; sodium hydroxide; acetic anhydride In methanol; toluene 12 Example 12 Example 12 Production of 3-[2,2-bis(1-n-octyl-2-methylindol-3-yl)ethenyl]-3-(4-diethylaminophenyl)phthalide First, 48.6 g (0.2 mole) of 1-n-octyl-2-methylindole, 7.85 g (0.1 mole) of acetyl chloride and 30 mL of acetic anhydride were stirred together at 50-55°C for 8 hours. Then, 7.4 g (0.1 mole) of calcium hydroxide, 29.7 g (0.1 mol) of 2-(4-diethylaminobenzoyl)benzoic acid and 50 mL of toluene were added and the mixture was stirred at 60-65°C for 4 hours. After cooling, 250 mL of toluene and 250 g of 10% aqueous sodium hydroxide solution were added and the mixture was stirred at reflux for 1 hour. The toluene layer was then taken, washed with warm water, filtered and concentrated. The residue was stirred with 200 mL of methanol at reflux for 1 hour. After cooling, the precipitate was recovered by filtration and dried to provide 47.8 g (yield 60.6%) of a pale greyish-white powder. m.p. 106-107°C. This product was identified as the object phthalide compound based on the following analyses. MS (m/z): 789 (M+)
  • 5
  • [ 111-86-4 ]
  • [ 21906-31-0 ]
  • [ 42951-39-3 ]
  • 6
  • C17H26BrN [ No CAS ]
  • [ 42951-39-3 ]
YieldReaction ConditionsOperation in experiment
90 mg With copper(l) iodide; K3PO4 In N,N-dimethyl-formamide at 110℃; Inert atmosphere;
  • 7
  • N-(2-chlorophenyl)octylamine [ No CAS ]
  • [ 67-64-1 ]
  • [ 42951-39-3 ]
YieldReaction ConditionsOperation in experiment
83% at 90℃; for 16h; Sealed tube; Inert atmosphere;
  • 8
  • [ 615-41-8 ]
  • [ 42951-39-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: C39H51ClNOPPd; N-[2-(di(1-adamantyl)phosphino)phenyl]morpholine; caesium carbonate / toluene / 6 h / 90 °C / Sealed tube; Inert atmosphere 2: 16 h / 90 °C / Sealed tube; Inert atmosphere
  • 9
  • [ 111-86-4 ]
  • [ 615-41-8 ]
  • [ 67-64-1 ]
  • [ 42951-39-3 ]
YieldReaction ConditionsOperation in experiment
44% With N-[2-(di(1-adamantyl)phosphino)phenyl]morpholine; C39H51ClNOPPd; caesium carbonate In toluene at 90℃; for 16h;
  • 10
  • [ 111-86-4 ]
  • [ 694-80-4 ]
  • [ 67-64-1 ]
  • [ 42951-39-3 ]
YieldReaction ConditionsOperation in experiment
62% With N-[2-(di(1-adamantyl)phosphino)phenyl]morpholine; C39H51ClNOPPd; caesium carbonate In toluene at 90℃; for 16h;
  • 11
  • [ 111-86-4 ]
  • [ 42951-39-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: C39H51ClNOPPd; N-[2-(di(1-adamantyl)phosphino)phenyl]morpholine; caesium carbonate / toluene / 6 h / 90 °C / Sealed tube; Inert atmosphere 2: 16 h / 90 °C / Sealed tube; Inert atmosphere
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