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[ CAS No. 80262-44-8 ] {[proInfo.proName]}

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Chemical Structure| 80262-44-8
Chemical Structure| 80262-44-8
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Product Details of [ 80262-44-8 ]

CAS No. :80262-44-8 MDL No. :MFCD05664716
Formula : C36H36N24O12 Boiling Point : No data available
Linear Structure Formula :- InChI Key :MSBXTPRURXJCPF-UHFFFAOYSA-N
M.W : 996.82 Pubchem ID :196163
Synonyms :

Safety of [ 80262-44-8 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 80262-44-8 ]

* 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 [ 80262-44-8 ]

[ 80262-44-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 496-46-8 ]
  • [ 17464-88-9 ]
  • [ 80262-44-8 ]
  • [ 259886-51-6 ]
  • [ 259886-50-5 ]
YieldReaction ConditionsOperation in experiment
Ca. 58%Spectr.; Ca. 9%Spectr.; Ca. 28%Spectr. With methanesulfonic acid; at 80 - 100℃; for 18.0h; Synthesis of cucurbit[n]urils in methanesulphonic acid usingTetramethoxymethylglycoluril (TMMG)Unsubstituted glycoluril (19.94 g) and methane sulphonic acid (neat, 82 ml_) were placed in a reaction flask and heated to 80 °C. TMMG (44.66 g) was added in drop-wise and the reaction mixture was then heated to 100 °C (internal temp) for 18 hours. The reaction mixture was cooled and added to methanol (410 ml) to produce a beige powder which was analysed by1H NMR. Approximate Yields b1H NMR (percent of recovered product) cucurbit[5]uri 5percent, cucurbit[6]uri 58percent, cucurbit[7]uril 28percent, cucurbit[8]uril 9percent, cucurbit[9]uril 0percent, cucurbit[10]uril 0percent, cucurbit[11]uril 0percent
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