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[ CAS No. 123-01-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 123-01-3
Chemical Structure| 123-01-3
Structure of 123-01-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 123-01-3 ]

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Product Details of [ 123-01-3 ]

CAS No. :123-01-3 MDL No. :MFCD00008974
Formula : C18H30 Boiling Point : -
Linear Structure Formula :H(CH2)12C6H5 InChI Key :KWKXNDCHNDYVRT-UHFFFAOYSA-N
M.W : 246.43 Pubchem ID :31237
Synonyms :
Chemical Name :Dodecylbenzene

Safety of [ 123-01-3 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P301+P312-P302+P352-P304+P340-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 123-01-3 ]

* 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 [ 123-01-3 ]

[ 123-01-3 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 5926-51-2 ]
  • [ 123-01-3 ]
  • [ 221632-48-0 ]
  • 2
  • [ 1122-12-9 ]
  • [ 123-01-3 ]
  • (Z)-2,3-Dibromo-4-(4-dodecyl-phenyl)-4-oxo-but-2-enoic acid [ No CAS ]
  • 3
  • [ 4292-19-7 ]
  • [ 5123-13-7 ]
  • [ 599-91-7 ]
  • [ 103-65-1 ]
  • [ 123-01-3 ]
  • 4
  • [ 5123-13-7 ]
  • [ 143-15-7 ]
  • [ 599-91-7 ]
  • [ 103-65-1 ]
  • [ 123-01-3 ]
  • 5
  • [ 5123-13-7 ]
  • [ 599-91-7 ]
  • [ 112-52-7 ]
  • [ 103-65-1 ]
  • [ 123-01-3 ]
  • 6
  • [ 56525-79-2 ]
  • [ 123-01-3 ]
  • [ 177775-88-1 ]
  • [ 1360431-76-0 ]
YieldReaction ConditionsOperation in experiment
38.5% Synthesis of 3,6-Diphenyl-9-tosyl-9H-carbazole 3-Bromo-9-tosyl-9H-carbazole (4.20 g, 13.2 mmol), <strong>[56525-79-2]3,6-diphenyl-9H-carbazole</strong> (4.87 g, 12.5 mmol) and copper(I) oxide (4.54 g, 31.8 mmol) were added to dodecylbenzene (12.3 mL), and the mixture was heated to 220°C under a nitrogen gas environment for 20 hours. After completing the reaction, copper (I) oxide was removed by filtration, and then the filtrate was purified by silica gel column chromatography (developing solvent: hexane/dichloromethane = 50/50) (yield amount: 3.24 g (5.07 mmol), yield: 38.5percent). 1H-NMR (500 MHz, CDCl3) : delta (ppm) 8.58 (d, J = 8.5 Hz, 1H), 8.43 (d, J = 1.5 Hz, 2H), 8.41 (d, J = 8.5 Hz, 1H), 8.14 (d, J = 2.0 Hz, 1H), 7.92 (d, J = 7.5 Hz, 1H), 7.84 (d, J = 8.5 Hz, 2H), 7.75-7.72 (m, 6H), 7.68 (dd, J = 1.5 Hz, J=2.0Hz, 2H), 7.59-7.56 (m, 1H), 7.52-7.45 (m, 5H), 7.42-7.39 (m, 1H), 7.37-7.35 (m, 2H), 2.34 (s, 3H)
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