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[ CAS No. 51344-12-8 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 51344-12-8
Chemical Structure| 51344-12-8
Chemical Structure| 51344-12-8
Structure of 51344-12-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 51344-12-8 ]

CAS No. :51344-12-8 MDL No. :MFCD18800941
Formula : C11H17NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :LTVRUDZZRDMXFX-UHFFFAOYSA-N
M.W : 195.26 Pubchem ID :15082317
Synonyms :

Safety of [ 51344-12-8 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313 UN#:N/A
Hazard Statements:H315-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 51344-12-8 ]

* 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 [ 51344-12-8 ]

[ 51344-12-8 ] Synthesis Path-Downstream   1~16

  • 1
  • [ 22921-76-2 ]
  • [ 124-40-3 ]
  • [ 51344-12-8 ]
YieldReaction ConditionsOperation in experiment
With ethanol at 120 - 130℃;
  • 2
  • [ 51344-12-8 ]
  • [ 75-03-6 ]
  • [ 137325-71-4 ]
YieldReaction ConditionsOperation in experiment
In diethyl ether Ambient temperature;
  • 3
  • [ 137325-67-8 ]
  • [ 51344-12-8 ]
YieldReaction ConditionsOperation in experiment
55% With lithium aluminium tetrahydride In diethyl ether Ambient temperature;
  • 4
  • [ 51344-12-8 ]
  • [ 74-88-4 ]
  • [2-(4-Methoxy-phenoxy)-ethyl]-trimethyl-ammonium; iodide [ No CAS ]
YieldReaction ConditionsOperation in experiment
In diethyl ether Ambient temperature;
  • 5
  • [ 51344-12-8 ]
  • [ 4101-68-2 ]
  • [ 2603-69-2 ]
YieldReaction ConditionsOperation in experiment
In butanone Heating;
  • 8
  • [ 51344-12-8 ]
  • {2-[4-(2-ethyl-7-methoxy-3-phenyl-quinolin-4-yloxy)-phenoxy]-ethyl}-dimethyl-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 7.26 mmol / BBr3 / CH2Cl2 / 4 h / 0 °C 2: NaOH / dimethylformamide / 110 °C
  • 9
  • [ 51344-12-8 ]
  • 4-[4-(2-dimethylamino-ethoxy)-phenoxy]-2-ethyl-3-phenyl-quinolin-7-ol [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: 7.26 mmol / BBr3 / CH2Cl2 / 4 h / 0 °C 2: NaOH / dimethylformamide / 110 °C 3: 0.0148 g / BBr3 / CH2Cl2 / 4 h / -20 - 20 °C
  • 10
  • [ 1877-75-4 ]
  • [ 51344-12-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: 4.2 g / SOCl2 / Ambient temperature 2: 80 percent / benzene; H2O / Ambient temperature 3: 55 percent / LiAlH4 / diethyl ether / Ambient temperature
  • 11
  • [ 42082-29-1 ]
  • [ 51344-12-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 80 percent / benzene; H2O / Ambient temperature 2: 55 percent / LiAlH4 / diethyl ether / Ambient temperature
  • 12
  • [ 150-76-5 ]
  • [ 51344-12-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: 39 percent / 6N NaOH / H2O / 2 h / Heating 2: 4.2 g / SOCl2 / Ambient temperature 3: 80 percent / benzene; H2O / Ambient temperature 4: 55 percent / LiAlH4 / diethyl ether / Ambient temperature
  • 13
  • [ 108-01-0 ]
  • [ 150-76-5 ]
  • [ 105-58-8 ]
  • [ 5076-72-2 ]
  • [ 51344-12-8 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate In acetonitrile at 200℃; for 8h; Autoclave;
  • 14
  • [ 20570-41-6 ]
  • [ 150-76-5 ]
  • [ 51344-12-8 ]
YieldReaction ConditionsOperation in experiment
96% In acetonitrile at 220℃; for 0.116667h; Sealed tube; Microwave irradiation; Reaction between 2-(dimethylamino)ethyl methyl carbonate 2 and phenol in ACN - Table 1, No.7 General procedure: Phenol (0.060 g, 0.637 mmol) was dissolved in ACN (3 mL) at room temperature in a 10 mL CEM pressure vessel equipped with a stirrer bar. 2-(Dimethylamino)ethyl methyl carbonate 2 (0.140 g, 0.955 mmol) was added and the vial was sealed and heated in a CEM Discover microwave synthesizer to 220 °C for 7 min. After cooling, a sample of the crude material was analysed by HPLC to define conversion and selectivity. Then, the reaction mixture was concentrated via rotavapor and it was purified via liquid-liquid extraction (EtOAc 50 mL / NaOH 5% aqueous solution 50 mL x 3). The organic phase was dried with sodium sulphate, filtered and concentrated under vacuum. The pure compound was isolated as a brown oil in 95% yield (0.100 g). Characterization of compound 3 was consistent with one reported in the literature.2
  • 15
  • [ 20570-41-6 ]
  • [ 150-76-5 ]
  • [ 67-63-0 ]
  • 2-(dimethylamino)ethyl isopropyl carbonate [ No CAS ]
  • [ 51344-12-8 ]
YieldReaction ConditionsOperation in experiment
at 220℃; for 0.116667h; Sealed tube; Microwave irradiation;
  • 16
  • [ 20570-41-6 ]
  • [ 150-76-5 ]
  • [ 71-36-3 ]
  • [ 51344-12-8 ]
  • butyl (2-(dimethylamino)ethyl) carbonate [ No CAS ]
YieldReaction ConditionsOperation in experiment
at 220℃; for 0.116667h; Sealed tube; Microwave irradiation;
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