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[ CAS No. 189373-41-9 ] {[proInfo.proName]}

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Chemical Structure| 189373-41-9
Chemical Structure| 189373-41-9
Structure of 189373-41-9 * Storage: {[proInfo.prStorage]}
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Product Details of [ 189373-41-9 ]

CAS No. :189373-41-9 MDL No. :MFCD01321129
Formula : C10H15N5O3S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 285.32 Pubchem ID :-
Synonyms :
Dbd-ed

Safety of [ 189373-41-9 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 189373-41-9 ]

* 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 [ 189373-41-9 ]

[ 189373-41-9 ] Synthesis Path-Downstream   1~9

  • 2
  • [ 189373-41-9 ]
  • [ 96-32-2 ]
  • [ 1048697-11-5 ]
YieldReaction ConditionsOperation in experiment
45% With potassium carbonate In acetonitrile at 70℃; for 6h;
  • 3
  • [ 189373-41-9 ]
  • [ 191108-03-9 ]
  • [ 1196721-53-5 ]
YieldReaction ConditionsOperation in experiment
With O‐(1H‐benzotriazol‐1‐yl)‐N,N,N′,N′‐tetramethyluronium tetrafluoroborate In acetonitrile at 20℃;
  • 4
  • [ 189373-41-9 ]
  • [ 24424-99-5 ]
  • [ 1334754-81-2 ]
YieldReaction ConditionsOperation in experiment
63% Stage #1: 7-((2-aminoethyl)amino)-N, N-dimethylbenzo[c][1, 2, 5]oxadiazole-4-sulfonamide With sodium hydroxide In chloroform; water for 0.25h; Stage #2: di-<i>tert</i>-butyl dicarbonate at 0 - 20℃;
  • 5
  • [ 189373-41-9 ]
  • [ 498568-17-5 ]
  • 7-((2-((1-(3-(1H-imidazol-1-yl)propyl)-4-benzoyl-5-(4-bromophenyl)-2-oxo-2,5-dihydro-1Hpyrrol-3-yl)amino)ethyl) amino)-N,N-dimethylbenzo[c][1,2,5]oxadiazole-4-sulfonamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
12.3% With acetic acid for 2h; Microwave irradiation;
  • 6
  • [ 7116-16-7 ]
  • [ 189373-41-9 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1.1: chlorosulfonic acid / 6 h / 120 - 130 °C 2.1: triethylamine / tetrahydrofuran / 0.5 h / 20 °C 2.2: 1 h / 0 °C 3.1: acetonitrile / 6 h / 60 °C
Multi-step reaction with 3 steps 1.1: chlorosulfonic acid / 6 h / 120 - 130 °C 2.1: triethylamine / tetrahydrofuran / 0.5 h / 20 °C 2.2: 1 h / 0 °C 3.1: acetonitrile / 6 h / 60 °C
  • 7
  • 7-chlorobenzo[c][1,2,5]oxadiazole-4-sulfonic acid chloride [ No CAS ]
  • [ 189373-41-9 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: triethylamine / tetrahydrofuran / 0.5 h / 20 °C 1.2: 1 h / 0 °C 2.1: acetonitrile / 6 h / 60 °C
  • 8
  • [ 189373-41-9 ]
  • C37H75NO16Si8 [ No CAS ]
  • C43H85N5O16SSi8 [ No CAS ]
YieldReaction ConditionsOperation in experiment
0.8 g With triethylamine In tetrahydrofuran for 23h; 4 In a 20 ml two-necked eggplant flask(N-succinimidyloxycarbonyl) isobutylsilsesquioxane(0.18 mmol) of the compound (2a)4- (N, N-dimethylaminosulfonyl) -7-(2-aminoethylamino) -2, 1, 3-benzoxadiazole, 51.2 mg (0.18 mmol)12 ml of dry THF was added and dissolved. Ten (10) drops of triethylamine were added, and the mixture was stirred for 23 hours.After stirring, the reaction solution was concentrated, dissolved in a mixed solvent of dichloromethane and methanol at 30 ° C., and slowly evaporated to obtain 0.80 g of a yellow-green solid.
  • 9
  • [ 189373-41-9 ]
  • 2-(4-(tert-butyl)-2-ethoxyphenyl)-4,5-bis(4-chlorophenyl)-4,5-dihydro-1H-imidazole-1-carbonyl chloride [ No CAS ]
  • C38H41Cl2N7O5S [ No CAS ]
YieldReaction ConditionsOperation in experiment
With triethylamine In dichloromethane at 20℃; for 0.5h;
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